A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6161354



Internal ID8812269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80200860..80204230hg38UCSC Ensembl
Outerchr9:80200703..80204383hg38UCSC Ensembl
Innerchr9:82815775..82819145hg19UCSC Ensembl
Outerchr9:82815618..82819298hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg383681
hg193681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663433
Supporting Variants
SamplesHG00256
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6161354
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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