A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527681



Internal ID15454974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101635667..101649954hg38UCSC Ensembl
Innerchr1:102101223..102115510hg19UCSC Ensembl
Innerchr1:101873811..101888098hg18UCSC Ensembl
Innerchr1:101813244..101827531hg17UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3814288
hg1914288
hg1814288
hg1714288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704157
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527681
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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