A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714008



Internal ID137674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63610988..63612164hg38UCSC Ensembl
chr17:61688348..61689524hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714008
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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