A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13516190



Internal ID4659661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72525463..72563122hg38UCSC Ensembl
Innerchr9:72525963..72562622hg38UCSC Ensembl
Outerchr9:72524463..72564122hg38UCSC Ensembl
chr9:75140379..75178038hg19UCSC Ensembl
Innerchr9:75140879..75177538hg19UCSC Ensembl
Outerchr9:75139379..75179038hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3837660
hg1937660
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620640
Supporting Variants
SamplesHG04186
Known GenesTMC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13516190
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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