A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213295



Internal ID20780335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150957723..150970386hg38UCSC Ensembl
chr5:150337285..150349948hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3812664
hg1912664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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