A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035060



Internal ID21944403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41657030..41657605hg38UCSC Ensembl
chr15:41949228..41949803hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035060
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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