A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829188



Internal ID22604123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214501076..214521673hg38UCSC Ensembl
chr1:214674419..214695016hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3820598
hg1920598
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469439
Samples
Known GenesPTPN14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829188
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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