A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397808



Internal ID21055361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63718790..63719365hg38UCSC Ensembl
chr6:64428686..64429261hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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