A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656232



Internal ID18954513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109568130..109635643hg38UCSC Ensembl
Innerchr7:109208187..109275700hg19UCSC Ensembl
Innerchr7:108995423..109062936hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3867514
hg1967514
hg1867514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020761
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)nssv3656232
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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