A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525634



Internal ID15452927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86961037..86979470hg38UCSC Ensembl
Innerchr7:86590353..86608786hg19UCSC Ensembl
Innerchr7:86428289..86446722hg18UCSC Ensembl
Innerchr7:86235004..86253437hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3818434
hg1918434
hg1818434
hg1718434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701788
Samples
Known GenesKIAA1324L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525634
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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