A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527496



Internal ID15454789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102143021..102261246hg38UCSC Ensembl
Innerchr1:102608577..102726802hg19UCSC Ensembl
Innerchr1:102381165..102499390hg18UCSC Ensembl
Innerchr1:102320598..102438823hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38118226
hg19118226
hg18118226
hg17118226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12n21
Supporting Variantsnssv703944
Samples
Known GenesMIR548AI
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527496
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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