A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605190



Internal ID20978261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139001925..139002405hg38UCSC Ensembl
chr6:139323062..139323542hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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