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Human Genome Issue HG-1068

Summary:
AC206420.3 has ~6kb of unique sequence to the Reference
Description:
AC206420.3 has 6,086bp unique sequence when compared to the Reference.
Status:
Resolved (GRC Resolved by Electronic Means)
Type:
Variation
Last updated:
2015-10-07
Affects version:
GRCh37
Fix version:
GRCh37.p3, GRCh37.p9, GRCh38
Resolution:
This patch involving AC206420.3 (ABC10-48936800O12) represents an alternate haplotype from GRCh37 component AC108512.4. It has a 6087 bp insertion relative to reference component AC108512.4.

Patches and alternate loci

Scaffold type:
ALT in GRCh37
Comment:
This scaffold involving AC206420.3 (ABC10-48936800O12) represents an alternate haplotype from GRCh37 component AC108512.4. It has a 6087 bp insertion relative to reference component AC108512.4.
Revision history of patches and alts for HG-1068
Assembly Scaffold type Contig name GenBank accession RefSeq accession Region
GRCh37.p3 NOVEL HSCHR2_2_CTG12 GL582966.1 NW_003571033.1 REGION44
GRCh37.p9 NOVEL HSCHR2_2_CTG12 GL582966.2 NW_003571033.2 REGION44
GRCh38 ALT HSCHR2_2_CTG7_2 GL582966.2 NW_003571033.2 REGION44

Locations and genomic context

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  • (View region: Ensembl | NCBI | UCSC)
  • (View region: Ensembl | NCBI | UCSC)