A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614949



Internal ID18913230
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 StatusS
Merged Variantsnsv1010962
Supporting Variants
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)nssv3614949
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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