A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1140625



Internal ID15993811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103548702..103603993hg38UCSC Ensembl
Innerchr9:106310984..106366275hg19UCSC Ensembl
Innerchr9:105350805..105406096hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3855292
hg1955292
hg1855292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615050
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1140625
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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