A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885929



Internal ID22660916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42378774..42424508hg38UCSC Ensembl
chr17:40530792..40576526hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3845735
hg1945735
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473790
Samples
Known GenesPTRF, STAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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