A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498708



Internal ID20871921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65817721..65821764hg38UCSC Ensembl
chr15:66110059..66114102hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384044
hg194044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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