A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562842



Internal ID335783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6017110..6094107hg38UCSC Ensembl
chr6:6017343..6094340hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3876998
hg1976998
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562842
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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