A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635972



Internal ID18934253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27651575..27708898hg38UCSC Ensembl
Innerchr5:27651682..27709005hg19UCSC Ensembl
Innerchr5:27687439..27744762hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3857324
hg1957324
hg1857324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026341
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)nssv3635972
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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