A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517698



Internal ID6014820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102725653..102776870hg19UCSC Ensembl
Innerchr10:102715643..102766860hg18UCSC Ensembl
Innerchr10:102715643..102766860hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv666988, nssv668656, nssv660862, nssv687630, nssv654660, nssv659735, nssv652885
Samples
Known GenesC10orf2, LZTS2, MIR608, MRPL43, PDZD7, SEMA4G
Method
AnalysisMerged-level CNV regions
PlatformIllumina HumanHap550 Genotyping BeadChip v3
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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