A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688166



Internal ID15424818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121009763..121030305hg38UCSC Ensembl
Innerchr10:122769276..122789818hg19UCSC Ensembl
Innerchr10:122759266..122779808hg18UCSC Ensembl
Innerchr10:122759266..122779808hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3820543
hg1920543
hg1820543
hg1720543
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516918
Supporting Variants
Samples
Known GenesMIR5694
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688166
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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