A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132255



Internal ID20699295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74780056..74780443hg38UCSC Ensembl
chr5:74075881..74076268hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396632
Supporting Variants
Samples
Known GenesFAM169A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00121


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