A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643371



Internal ID18941652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32171302..32383787hg38UCSC Ensembl
Innerchr7:32210914..32423399hg19UCSC Ensembl
Innerchr7:32177439..32389924hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38212486
hg19212486
hg18212486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028414
Supporting Variants
Samples
Known GenesPDE1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643371
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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