A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138490



Internal ID20705530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139503865..139516356hg38UCSC Ensembl
chr6:139825002..139837493hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3812492
hg1912492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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