A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551551



Internal ID15992274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77261063..77359691hg38UCSC Ensembl
Innerchr10:79020821..79119449hg19UCSC Ensembl
Innerchr10:78690827..78789455hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3898629
hg1998629
hg1898629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751733
Samples
Known GenesKCNMA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551551
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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