A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13633379



Internal ID6272352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131960222..131965102hg38UCSC Ensembl
Innerchr9:131960372..131964952hg38UCSC Ensembl
Outerchr9:131960072..131965252hg38UCSC Ensembl
chr9:134835609..134840489hg19UCSC Ensembl
Innerchr9:134835759..134840339hg19UCSC Ensembl
Outerchr9:134835459..134840639hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384881
hg194881
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621904
Supporting Variants
SamplesNA19789
Known GenesMED27
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13633379
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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