A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398058



Internal ID21055611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65836424..65836941hg38UCSC Ensembl
chr6:66546317..66546834hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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