A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522412



Internal ID15449705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64139247..64429331hg38UCSC Ensembl
Innerchr7:63599625..63889709hg19UCSC Ensembl
Innerchr7:63237060..63527144hg18UCSC Ensembl
Innerchr7:63043775..63333859hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38290085
hg19290085
hg18290085
hg17290085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695195
Samples
Known GenesZNF679, ZNF735, ZNF736
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522412
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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