A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521064



Internal ID15448357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149086005..149092197hg38UCSC Ensembl
Innerchr2:149942519..149948711hg19UCSC Ensembl
Innerchr2:149650765..149656957hg18UCSC Ensembl
Innerchr2:149768027..149774219hg17UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg386193
hg196193
hg186193
hg176193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv230n21
Supporting Variantsnssv697765
Samples
Known GenesLYPD6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521064
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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