A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704288



Internal ID15440940
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527796
Supporting Variants
Samples
Known GenesLYPD6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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