A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133128



Internal ID20700168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60391526..60392025hg38UCSC Ensembl
chr5:59687353..59687852hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411960
Supporting Variants
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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