A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550870



Internal ID15991593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51615660..51681247hg38UCSC Ensembl
Innerchr10:53375420..53441007hg19UCSC Ensembl
Innerchr10:53045426..53111013hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3865588
hg1965588
hg1865588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1133n54
Supporting Variantsnssv747851
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550870
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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