A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023665



Internal ID19112882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11417866..11733890hg38UCSC Ensembl
Innerchr7:11457493..11773517hg19UCSC Ensembl
Innerchr7:11424018..11740042hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38316025
hg19316025
hg18316025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752889
Samples
Known GenesTHSD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023665
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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