A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397694



Internal ID21055247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95979332..95992414hg38UCSC Ensembl
chr6:96427208..96440290hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3813083
hg1913083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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