A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527283



Internal ID15107890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103374133..103586151hg38UCSC Ensembl
Innerchr1:103916755..104128773hg19UCSC Ensembl
Innerchr1:103689343..103930296hg18UCSC Ensembl
Innerchr1:103628776..103840794hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38212019
hg19212019
hg18240954
hg17212019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14n21
Supporting Variantsnssv703695
Samples
Known GenesACTG1P4, AMY2B, LOC101928436, RNPC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527283
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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