A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662117



Internal ID18960398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122130387..122180676hg38UCSC Ensembl
Innerchr7:121770441..121820730hg19UCSC Ensembl
Innerchr7:121557677..121607966hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3850290
hg1950290
hg1850290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016617
Supporting Variants
Samples
Known GenesAASS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662117
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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