A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705873



Internal ID15095839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18164280..18176550hg38UCSC Ensembl
Innerchr10:18453209..18465479hg19UCSC Ensembl
Innerchr10:18493215..18505485hg18UCSC Ensembl
Innerchr10:18493215..18505485hg17UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3812271
hg1912271
hg1812271
hg1712271
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522505
Supporting Variants
Samples
Known GenesCACNB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705873
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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