A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3617016



Internal ID18568611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197516065..197581406hg38UCSC Ensembl
Innerchr3:197242936..197308277hg19UCSC Ensembl
Innerchr3:198727333..198792674hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3865342
hg1965342
hg1865342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006202
Supporting Variants
Samples
Known GenesBDH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3617016
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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