A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025941



Internal ID18768473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76550385..76912763hg38UCSC Ensembl
Innerchr7:76179702..76542080hg19UCSC Ensembl
Innerchr7:76017638..76380016hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38362379
hg19362379
hg18362379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6473n100
Supporting Variantsnssv3656617
Samples
Known GenesLOC100133091, POMZP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025941
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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