A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128703



Internal ID20695743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151388840..151391158hg38UCSC Ensembl
chr5:150768401..150770719hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382319
hg192319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128703
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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