A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954962



Internal ID21375032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15942538..15942885hg38UCSC Ensembl
chr5:15942647..15942994hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195831
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954962
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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