A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577239



Internal ID18875520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57987736..58089012hg38UCSC Ensembl
Innerchr2:58214871..58316147hg19UCSC Ensembl
Innerchr2:58068375..58169651hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38101277
hg19101277
hg18101277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999591
Supporting Variants
Samples
Known GenesVRK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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