A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563403



Internal ID336337
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 StatusM
Merged Variants
Supporting Variantsnssv17724211
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)nsv5563403
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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