A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562394



Internal ID335350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99913224..99940026hg38UCSC Ensembl
chr7:99510847..99537649hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3826803
hg1926803
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002927
Samples
Known GenesGJC3, TRIM4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562394
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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