A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395699



Internal ID21053252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8788585..8789108hg38UCSC Ensembl
chr6:8788818..8789341hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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