A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525995



Internal ID15106602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79305444..79309656hg38UCSC Ensembl
Innerchr10:81065201..81069413hg19UCSC Ensembl
Innerchr10:80735207..80739419hg18UCSC Ensembl
Innerchr10:80735207..80739419hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384213
hg194213
hg184213
hg174213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702220
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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