A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554691



Internal ID327869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2997997..3056987hg38UCSC Ensembl
chr6:2998231..3057221hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3858991
hg1958991
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977976
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554691
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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