A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526581



Internal ID302708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11291226..11292885hg38UCSC Ensembl
chr17:11194543..11196202hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381660
hg191660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711433
Samples
Known GenesSHISA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526581
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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