A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014852



Internal ID19104069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21943888..21968594hg38UCSC Ensembl
Innerchr3:21985380..22010086hg19UCSC Ensembl
Innerchr3:21960384..21985090hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3824707
hg1924707
hg1824707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4697n100
Supporting Variantsnssv3589452, nssv3589451, nssv3589449, nssv3589450
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)nsv1014852
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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