A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529027



Internal ID15109634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37108500..37353255hg38UCSC Ensembl
Innerchr9:37108497..37353252hg19UCSC Ensembl
Innerchr9:37098497..37343252hg18UCSC Ensembl
Innerchr9:37098497..37343252hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38244756
hg19244756
hg18244756
hg17244756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705738
Samples
Known GenesZCCHC7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529027
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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