A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035064



Internal ID91110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48251776..48281663hg38UCSC Ensembl
chr10:49459819..49489706hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3829888
hg1929888
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554295
Supporting Variants
Samples
Known GenesFRMPD2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035064
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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