A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527682



Internal ID15108289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:155177242..155227671hg38UCSC Ensembl
Innerchr1:155149718..155197462hg19UCSC Ensembl
Innerchr1:153416342..153464086hg18UCSC Ensembl
Innerchr1:151962791..152010535hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3850430
hg1947745
hg1847745
hg1747745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704158
Samples
Known GenesGBAP1, MIR92B, MTX1, MUC1, THBS3, TRIM46
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527682
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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