A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662142



Internal ID18960423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124951379..125028369hg38UCSC Ensembl
Innerchr7:124591433..124668423hg19UCSC Ensembl
Innerchr7:124378669..124455659hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3876991
hg1976991
hg1876991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025873
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)nssv3662142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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