A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555899



Internal ID329048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15962066..16010762hg38UCSC Ensembl
chr17:15865380..15914076hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3848697
hg1948697
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711747
Samples
Known GenesADORA2B, TTC19, ZSWIM7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555899
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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