A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497180



Internal ID20870385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55174726..55175119hg38UCSC Ensembl
chr15:55466924..55467317hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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