A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507903



Internal ID20881199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24095597..24470955hg38UCSC Ensembl
chr15:24340744..24716102hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38375359
hg19375359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2397n223
Supporting Variantsnssv18022856
Samples
Known GenesPWRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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