A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523996



Internal ID15451289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74806926..74813324hg38UCSC Ensembl
Innerchr18:72518882..72525280hg19UCSC Ensembl
Innerchr18:70647870..70654268hg18UCSC Ensembl
Innerchr18:70647870..70654268hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg386399
hg196399
hg186399
hg176399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699856
Samples
Known GenesZNF407
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523996
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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