A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013158



Internal ID19102376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176177207..176219130hg38UCSC Ensembl
Innerchr3:175894995..175936918hg19UCSC Ensembl
Innerchr3:177377689..177419612hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3841924
hg1941924
hg1841924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4991n100
Supporting Variantsnssv3614939, nssv3614941, nssv3614940, nssv3614942, nssv3614938, nssv3614935, nssv3614944, nssv3614943, nssv3614945, nssv3614936, nssv3614937
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)nsv1013158
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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