A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012654



Internal ID19101871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21218878..21302104hg38UCSC Ensembl
Innerchr3:21260370..21343596hg19UCSC Ensembl
Innerchr3:21235374..21318600hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3883227
hg1983227
hg1883227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4690n100
Supporting Variantsnssv3593139, nssv3593138, nssv3593140, nssv3593141
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)nsv1012654
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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