A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562263



Internal ID335221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11414853..11423572hg38UCSC Ensembl
chr6:11415086..11423805hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg388720
hg198720
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562263
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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