A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401731



Internal ID21059284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23598104..23614048hg38UCSC Ensembl
chr6:23598332..23614276hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3815945
hg1915945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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