A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576653



Internal ID18874934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:55097140..55117190hg38UCSC Ensembl
Innerchr2:55324276..55344326hg19UCSC Ensembl
Innerchr2:55177780..55197830hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3820051
hg1920051
hg1820051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997458
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)nssv3576653
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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