A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3494236



Internal ID19081877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:187677276..187804078hg38UCSC Ensembl
Innerchr1:187646408..187773209hg19UCSC Ensembl
Innerchr1:185913031..186039832hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38126803
hg19126802
hg18126802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011007
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3494236
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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