A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703735



Internal ID15093701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133556501..133620799hg38UCSC Ensembl
Innerchr10:135370005..135434303hg19UCSC Ensembl
Innerchr10:135219995..135284293hg18UCSC Ensembl
Innerchr10:135258886..135323184hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3864299
hg1964299
hg1864299
hg1764299
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517180
Supporting Variants
Samples
Known GenesSPRNP1, SYCE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703735
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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