A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724211



Internal ID147877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52689727..53366381hg38UCSC Ensembl
chr19:53192980..53869634hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38676655
hg19676655
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563403
Supporting Variants
Samples
Known GenesBIRC8, ERVV-1, ERVV-2, FAM90A27P, VN1R2, VN1R4, ZNF160, ZNF28, ZNF320, ZNF321P, ZNF347, ZNF415, ZNF468, ZNF525, ZNF600, ZNF611, ZNF665, ZNF677, ZNF702P, ZNF816, ZNF816-ZNF321P, ZNF818P, ZNF83, ZNF845
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724211
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.284421


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