A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011023



Internal ID22072654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33613874..33616769hg38UCSC Ensembl
Outerchr15:33608504..33619636hg38UCSC Ensembl
Innerchr15:33906075..33908970hg19UCSC Ensembl
Outerchr15:33900705..33911837hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811133
hg1911133
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155154
Supporting Variants
Samples
Known GenesRYR3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011023
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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