A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660862



Internal ID15050828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100965896..101010325hg38UCSC Ensembl
Innerchr10:102725653..102770082hg19UCSC Ensembl
Innerchr10:102715643..102760072hg18UCSC Ensembl
Innerchr10:102715643..102760072hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3844430
hg1944430
hg1844430
hg1744430
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517698
Supporting Variants
Samples
Known GenesC10orf2, LZTS2, MIR608, MRPL43, PDZD7, SEMA4G
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660862
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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