A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560567



Internal ID333573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109802242..110580747hg38UCSC Ensembl
chr13:110454589..111233094hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38778506
hg19778506
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695568
Samples
Known GenesCOL4A1, COL4A2, COL4A2-AS1, MIR8073, RAB20
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560567
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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