A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601989



Internal ID20975060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163497722..163522957hg38UCSC Ensembl
chr6:163918754..163943989hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3825236
hg1925236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142255
Samples
Known GenesQKI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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