A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034063



Internal ID90408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63414652..63419138hg38UCSC Ensembl
chr10:65174412..65178898hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384487
hg194487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492917
Supporting Variants
Samples
Known GenesJMJD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034063
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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