A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13573015



Internal ID3574831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96634094..96634599hg38UCSC Ensembl
Innerchr9:96634101..96634592hg38UCSC Ensembl
Outerchr9:96634087..96634606hg38UCSC Ensembl
chr9:99396376..99396881hg19UCSC Ensembl
Innerchr9:99396383..99396874hg19UCSC Ensembl
Outerchr9:99396369..99396888hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621169
Supporting Variants
SamplesHG03295
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13573015
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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