A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504713



Internal ID20877976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39335535..39346876hg38UCSC Ensembl
chr15:39627736..39639077hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811342
hg1911342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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