A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005915



Internal ID19095133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91608646hg38UCSC Ensembl
Innerchr2:91618895..91796672hg19UCSC Ensembl
Innerchr2:90982622..91160399hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38182121
hg19177778
hg18177778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3990n100
Supporting Variantsnssv3579413, nssv3579412
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)nsv1005915
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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