A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559038



Internal ID332084
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 StatusM
Merged Variants
Supporting Variantsnssv17714008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559038
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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