A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497538



Internal ID20870745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92487988..92488593hg38UCSC Ensembl
chr15:93031218..93031823hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027299
Samples
Known GenesC15orf32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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