A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537122



Internal ID312473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:185635..185686hg38UCSC Ensembl
chr6:185635..185686hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537122
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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