A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010962



Internal ID19100179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176177543..176219130hg38UCSC Ensembl
Innerchr3:175895331..175936918hg19UCSC Ensembl
Innerchr3:177378025..177419612hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3841588
hg1941588
hg1841588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4991n100
Supporting Variantsnssv3614949
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)nsv1010962
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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