A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13513851



Internal ID4529402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71204956..71244562hg38UCSC Ensembl
Innerchr9:71204956..71244562hg38UCSC Ensembl
Outerchr9:71204456..71245062hg38UCSC Ensembl
chr9:73819872..73859478hg19UCSC Ensembl
Innerchr9:73819872..73859478hg19UCSC Ensembl
Outerchr9:73819372..73859978hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3839607
hg1939607
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620603
Supporting Variants
SamplesHG04023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13513851
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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