A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499330



Internal ID20872549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80352457..80352991hg38UCSC Ensembl
chr15:80644799..80645333hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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