A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127491



Internal ID20694531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160182745..160189342hg38UCSC Ensembl
chr5:159609752..159616349hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg386598
hg196598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414196
Supporting Variants
Samples
Known GenesFABP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127491
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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