A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174545



Internal ID15507848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51628463..51681247hg38UCSC Ensembl
Innerchr10:53388223..53441007hg19UCSC Ensembl
Innerchr10:53058229..53111013hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3852785
hg1952785
hg1852785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550871
Supporting Variants
Samples1780862194_A
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174545
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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