A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549976



Internal ID15990699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12775196..12775992hg38UCSC Ensembl
Innerchr10:12817195..12817991hg19UCSC Ensembl
Innerchr10:12857201..12857997hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38797
hg19797
hg18797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744013
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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