A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557306



Internal ID330406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16372615..16575020hg38UCSC Ensembl
chr17:16275929..16478334hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38202406
hg19202406
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711782
Samples
Known GenesFAM211A, FAM211A-AS1, SNORD49A, SNORD49B, SNORD65, TRPV2, UBB, ZNF287
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557306
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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