A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137088



Internal ID20704128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113746398..113751143hg38UCSC Ensembl
chr6:114067600..114072345hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384746
hg194746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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