A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009629



Internal ID20576669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50698488..50708009hg38UCSC Ensembl
chr13:51272624..51282145hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg389522
hg199522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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