A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195824



Internal ID21334620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13855191..13855506hg38UCSC Ensembl
chr5:13855300..13855615hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949988
Supporting Variants
SamplesHG002
Known GenesDNAH5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195824
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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