A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13515757



Internal ID1528891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71949584..71960757hg38UCSC Ensembl
Innerchr9:71949619..71960722hg38UCSC Ensembl
Outerchr9:71949549..71960792hg38UCSC Ensembl
chr9:74564500..74575673hg19UCSC Ensembl
Innerchr9:74564535..74575638hg19UCSC Ensembl
Outerchr9:74564465..74575708hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3811174
hg1911174
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620620
Supporting Variants
SamplesHG01402
Known GenesC9orf85
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13515757
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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