A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504137



Internal ID20877398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31168001..31169500hg38UCSC Ensembl
chr15:31460204..31461703hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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