A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527217



Internal ID15107824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10033399..10197109hg38UCSC Ensembl
Innerchr1:10093457..10257167hg19UCSC Ensembl
Innerchr1:10016044..10179754hg18UCSC Ensembl
Innerchr1:10027723..10191433hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38163711
hg19163711
hg18163711
hg17163711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703617
Samples
Known GenesUBE4B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527217
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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