A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399184



Internal ID21056737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95723851..95741414hg38UCSC Ensembl
chr6:96171727..96189290hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3817564
hg1917564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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