A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687167



Internal ID15423819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121010375..121024758hg38UCSC Ensembl
Innerchr10:122769888..122784271hg19UCSC Ensembl
Innerchr10:122759878..122774261hg18UCSC Ensembl
Innerchr10:122759878..122774261hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3814384
hg1914384
hg1814384
hg1714384
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)nssv687167
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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