A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138810



Internal ID20705850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118934301..118935100hg38UCSC Ensembl
chr6:119255466..119256265hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602916
Supporting Variants
Samples
Known GenesMCM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.06452


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