A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13513836



Internal ID4529021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71144707..71180476hg38UCSC Ensembl
Innerchr9:71144707..71180476hg38UCSC Ensembl
Outerchr9:71144207..71180976hg38UCSC Ensembl
chr9:73759623..73795392hg19UCSC Ensembl
Innerchr9:73759623..73795392hg19UCSC Ensembl
Outerchr9:73759123..73795892hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3835770
hg1935770
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620599
Supporting Variants
SamplesHG04023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13513836
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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