A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555695



Internal ID328846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34537631..34749387hg38UCSC Ensembl
chr19:35028536..35240292hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38211757
hg19211757
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722949
Samples
Known GenesSCGB1B2P, SCGB2B2, SCGB2B3P, ZNF181, ZNF302
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555695
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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