A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13591900



Internal ID4734766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104717697..104729043hg38UCSC Ensembl
Innerchr9:104717726..104729014hg38UCSC Ensembl
Outerchr9:104717668..104729072hg38UCSC Ensembl
chr9:107479978..107491324hg19UCSC Ensembl
Innerchr9:107480007..107491295hg19UCSC Ensembl
Outerchr9:107479949..107491353hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3811347
hg1911347
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621341
Supporting Variants
SamplesNA07000
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13591900
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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