A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408176



Internal ID21065729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89171197..89171964hg38UCSC Ensembl
chr6:89880916..89881683hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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