A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6452671



Internal ID9393098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21320589..21321463hg38UCSC Ensembl
Outerchr10:21320552..21321513hg38UCSC Ensembl
Innerchr10:21609518..21610392hg19UCSC Ensembl
Outerchr10:21609481..21610442hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663592
Supporting Variants
SamplesNA18596
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6452671
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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