A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666988



Internal ID15056954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100986746..101017113hg38UCSC Ensembl
Innerchr10:102746503..102776870hg19UCSC Ensembl
Innerchr10:102736493..102766860hg18UCSC Ensembl
Innerchr10:102736493..102766860hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3830368
hg1930368
hg1830368
hg1730368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517698
Supporting Variants
Samples
Known GenesC10orf2, LZTS2, MRPL43, PDZD7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666988
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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