A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729772



Internal ID19028053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88844243..88989522hg38UCSC Ensembl
Innerchr2:89143756..89289041hg19UCSC Ensembl
Innerchr2:88924871..89070156hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38145280
hg19145286
hg18145286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003064
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)nssv3729772
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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