A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516924



Internal ID15444217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41340348..41359612hg38UCSC Ensembl
Innerchr20:39968988..39988252hg19UCSC Ensembl
Innerchr20:39402402..39421666hg18UCSC Ensembl
Innerchr20:39402402..39421666hg17UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3819265
hg1919265
hg1819265
hg1719265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv245n21
Supporting Variantsnssv660837, nssv663362, nssv680715, nssv655006, nssv660059, nssv687498, nssv678146, nssv657691
Samples
Known GenesLPIN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516924
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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