A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560662



Internal ID333665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231559018..231559804hg38UCSC Ensembl
chr1:231694764..231695550hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16896424
Samples
Known GenesTSNAX, TSNAX-DISC1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560662
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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