A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018826



Internal ID18761359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76514308..76867835hg38UCSC Ensembl
Innerchr7:76143625..76497152hg19UCSC Ensembl
Innerchr7:75981561..76335088hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38353528
hg19353528
hg18353528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6473n100
Supporting Variantsnssv3656556
Samples
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018826
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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