A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662043



Internal ID18960324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:115524513..115581115hg38UCSC Ensembl
Innerchr7:115164567..115221169hg19UCSC Ensembl
Innerchr7:114951803..115008405hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3856603
hg1956603
hg1856603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030920
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)nssv3662043
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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