A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009761



Internal ID19098980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90071897hg38UCSC Ensembl
Innerchr2:89934947..90110739hg19UCSC Ensembl
Innerchr2:89571989..89748044hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38175761
hg19175793
hg18176056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3579785, nssv3579786
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)nsv1009761
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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