A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659700



Internal ID15396352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121010375..121025489hg38UCSC Ensembl
Innerchr10:122769888..122785002hg19UCSC Ensembl
Innerchr10:122759878..122774992hg18UCSC Ensembl
Innerchr10:122759878..122774992hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3815115
hg1915115
hg1815115
hg1715115
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)nssv659700
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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