A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619879



Internal ID20992950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96569438..96571681hg38UCSC Ensembl
chr6:97017314..97019557hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg382244
hg192244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150486
Samples
Known GenesFHL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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