A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999212



Internal ID19158748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:55097140..55113676hg38UCSC Ensembl
Innerchr2:55324276..55340812hg19UCSC Ensembl
Innerchr2:55177780..55194316hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3816537
hg1916537
hg1816537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3849n100
Supporting Variantsnssv3576651, nssv3576648, nssv3576649, nssv3576650
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)nsv999212
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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