A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137967



Internal ID20705007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119839173..119839677hg38UCSC Ensembl
chr6:120160319..120160823hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137967
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00267


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