A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527796



Internal ID15455089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149086005..149091549hg38UCSC Ensembl
Innerchr2:149942519..149948063hg19UCSC Ensembl
Innerchr2:149650765..149656309hg18UCSC Ensembl
Innerchr2:149768027..149773571hg17UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg385545
hg195545
hg185545
hg175545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv230n21
Supporting Variantsnssv704288
Samples
Known GenesLYPD6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527796
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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