A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643330



Internal ID18941611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:29229518..29352917hg38UCSC Ensembl
Innerchr7:29269134..29392533hg19UCSC Ensembl
Innerchr7:29235659..29359058hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38123400
hg19123400
hg18123400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034932
Supporting Variants
Samples
Known GenesCHN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643330
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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