A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596272



Internal ID18894553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:85485409..85580996hg38UCSC Ensembl
Innerchr3:85534559..85630146hg19UCSC Ensembl
Innerchr3:85617249..85712836hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3895588
hg1995588
hg1895588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002139
Supporting Variants
Samples
Known GenesCADM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596272
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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