A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576600



Internal ID18874881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52733215..52942479hg38UCSC Ensembl
Innerchr2:52960353..53169617hg19UCSC Ensembl
Innerchr2:52813857..53023121hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38209265
hg19209265
hg18209265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014068
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)nssv3576600
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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