A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129433



Internal ID20696473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155734442..155740461hg38UCSC Ensembl
chr5:155114002..155120021hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg386020
hg196020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00043


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