A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516914



Internal ID15097521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124483043..124484987hg38UCSC Ensembl
Innerchr10:126171612..126173556hg19UCSC Ensembl
Innerchr10:126161602..126163546hg18UCSC Ensembl
Innerchr10:126161602..126163546hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381945
hg191945
hg181945
hg171945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654943, nssv673647
Samples
Known GenesLHPP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516914
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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