A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522754



Internal ID15450047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:115225843..115245602hg38UCSC Ensembl
Innerchr2:115983419..116003178hg19UCSC Ensembl
Innerchr2:115699889..115719648hg18UCSC Ensembl
Innerchr2:115699649..115719408hg17UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3819760
hg1919760
hg1819760
hg1719760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698391
Samples
Known GenesDPP10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522754
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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