A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635965



Internal ID18934246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27143176..27199483hg38UCSC Ensembl
Innerchr5:27143283..27199590hg19UCSC Ensembl
Innerchr5:27179040..27235347hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3856308
hg1956308
hg1856308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025795
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)nssv3635965
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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