A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556991



Internal ID330109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35695141..35695147hg38UCSC Ensembl
chr13:36269278..36269284hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg387
hg197
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686857
Samples
Known GenesMIR548F5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556991
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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