A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635944



Internal ID18587539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:23407127..23686843hg38UCSC Ensembl
Innerchr5:23407236..23686952hg19UCSC Ensembl
Innerchr5:23442993..23722709hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg38279717
hg19279717
hg18279717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028347
Supporting Variants
Samples
Known GenesPRDM9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635944
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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