A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15196063



Internal ID21334859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40800767..40800893hg38UCSC Ensembl
chr5:40800869..40800995hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942774
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15196063
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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