A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616335



Internal ID20989406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108379955..108382324hg38UCSC Ensembl
chr6:108701159..108703528hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382370
hg192370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136991
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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