A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521187



Internal ID15101794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105311508..105352623hg38UCSC Ensembl
Innerchr8:106323736..106364851hg19UCSC Ensembl
Innerchr8:106392912..106434027hg18UCSC Ensembl
Innerchr8:106392912..106434027hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3841116
hg1941116
hg1841116
hg1741116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697834
Samples
Known GenesZFPM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521187
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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