A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500363



Internal ID20873589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40970592..40975484hg38UCSC Ensembl
chr15:41262790..41267682hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384893
hg194893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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