A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131736



Internal ID20698776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55149401..55150200hg38UCSC Ensembl
chr5:54445229..54446028hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410305
Supporting Variants
Samples
Known GenesCDC20B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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