A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399217



Internal ID21056770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3895424..3897424hg38UCSC Ensembl
chr6:3895658..3897658hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382001
hg192001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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