A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019074



Internal ID19108291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132883495..132926618hg38UCSC Ensembl
Innerchr7:132568255..132611378hg19UCSC Ensembl
Innerchr7:132218795..132261918hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3843124
hg1943124
hg1843124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751543
Samples
Known GenesCHCHD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019074
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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