A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519110



Internal ID15446403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:91328691..91335389hg38UCSC Ensembl
Innerchr1:91794248..91800946hg19UCSC Ensembl
Innerchr1:91566836..91573534hg18UCSC Ensembl
Innerchr1:91506269..91512967hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg386699
hg196699
hg186699
hg176699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696586
Samples
Known GenesHFM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519110
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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