A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654660



Internal ID15044626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100986746..101012526hg38UCSC Ensembl
Innerchr10:102746503..102772283hg19UCSC Ensembl
Innerchr10:102736493..102762273hg18UCSC Ensembl
Innerchr10:102736493..102762273hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3825781
hg1925781
hg1825781
hg1725781
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)nssv654660
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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