A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048555



Internal ID20615595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57147872..57161410hg38UCSC Ensembl
chr19:57659240..57672778hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3813539
hg1913539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532740
Supporting Variants
Samples
Known GenesDUXA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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