A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680611



Internal ID15070577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44892949hg38UCSC Ensembl
Innerchr10:45210690..45388397hg19UCSC Ensembl
Innerchr10:44530696..44708403hg18UCSC Ensembl
Innerchr10:44530696..44708403hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38177708
hg19177708
hg18177708
hg17177708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517161
Supporting Variants
Samples
Known GenesTMEM72-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680611
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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