A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498090



Internal ID20871298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25755601..25761300hg38UCSC Ensembl
chr15:26000748..26006447hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024294
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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