A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495806



Internal ID20869001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37975382..37976110hg38UCSC Ensembl
chr15:38267583..38268311hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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