A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676621



Internal ID9942726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48348320..48355855hg38UCSC Ensembl
Outerchr15:48348163..48356008hg38UCSC Ensembl
Innerchr15:48640517..48648052hg19UCSC Ensembl
Outerchr15:48640360..48648205hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg387846
hg197846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6441096, essv5537090
SamplesNA12763, HG00329
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676621
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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