A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517698



Internal ID8411973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100965896..101017113hg38UCSC Ensembl
Innerchr10:102725653..102776870hg19UCSC Ensembl
Innerchr10:102715643..102766860hg18UCSC Ensembl
Innerchr10:102715643..102766860hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3851218
hg1951218
hg1851218
hg1751218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666988, nssv668656, nssv660862, nssv687630, nssv654660, nssv659735, nssv652885
Samples
Known GenesC10orf2, LZTS2, MIR608, MRPL43, PDZD7, SEMA4G
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517698
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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