A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13553996



Internal ID6888219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90313683..90316631hg38UCSC Ensembl
Innerchr9:90313706..90316608hg38UCSC Ensembl
Outerchr9:90313660..90316654hg38UCSC Ensembl
chr9:93075965..93078913hg19UCSC Ensembl
Innerchr9:93075988..93078890hg19UCSC Ensembl
Outerchr9:93075942..93078936hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382949
hg192949
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621043
Supporting Variants
SamplesNA21104
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13553996
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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