A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525216



Internal ID15452509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10135882..10140516hg38UCSC Ensembl
Innerchr1:10195940..10200574hg19UCSC Ensembl
Innerchr1:10118527..10123161hg18UCSC Ensembl
Innerchr1:10130206..10134840hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384635
hg194635
hg184635
hg174635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701302
Samples
Known GenesUBE4B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525216
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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