A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397967



Internal ID21055520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3691208..3711367hg38UCSC Ensembl
chr6:3691442..3711601hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3820160
hg1920160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397967
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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