A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876944



Internal ID22651907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67598009..67608610hg38UCSC Ensembl
chr17:65594125..65604726hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3810602
hg1910602
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475837
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876944
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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