A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476732



Internal ID22534630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46134253..46141418hg38UCSC Ensembl
chr19:46637510..46644675hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg387166
hg197166
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872307
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476732
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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