A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662648



Internal ID15052614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715242..44873696hg38UCSC Ensembl
Innerchr10:45210690..45369144hg19UCSC Ensembl
Innerchr10:44530696..44689150hg18UCSC Ensembl
Innerchr10:44530696..44689150hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38158455
hg19158455
hg18158455
hg17158455
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)nssv662648
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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