A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498012



Internal ID20871220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54834961..54891853hg38UCSC Ensembl
chr15:55127159..55184051hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3856893
hg1956893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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