A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137270



Internal ID20704310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117863729..117867806hg38UCSC Ensembl
chr6:118184892..118188969hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg384078
hg194078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137270
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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