A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15180261



Internal ID21319057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815475..4815805hg38UCSC Ensembl
chr10:4857667..4857997hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954586
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15180261
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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