A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524847



Internal ID15105454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71745256..71772339hg38UCSC Ensembl
Innerchr3:71794407..71821490hg19UCSC Ensembl
Innerchr3:71877097..71904180hg18UCSC Ensembl
Innerchr3:71877097..71904180hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3827084
hg1927084
hg1827084
hg1727084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700849
Samples
Known GenesEIF4E3, GPR27, PROK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524847
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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