A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516847



Internal ID15444140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66377858..66387532hg38UCSC Ensembl
Innerchr3:66428282..66437956hg19UCSC Ensembl
Innerchr3:66510972..66520646hg18UCSC Ensembl
Innerchr3:66510972..66520646hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg389675
hg199675
hg189675
hg179675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654408, nssv684736
Samples
Known GenesLRIG1, SLC25A26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516847
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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