A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497239



Internal ID20870444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49976465..49977405hg38UCSC Ensembl
chr15:50268662..50269602hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38941
hg19941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025147
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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