A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551552



Internal ID15992275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77637709..77638858hg38UCSC Ensembl
Innerchr10:79397467..79398616hg19UCSC Ensembl
Innerchr10:79067473..79068622hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381150
hg191150
hg181150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751734
Samples
Known GenesKCNMA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551552
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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