A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886018



Internal ID22661005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21309603..21317803hg38UCSC Ensembl
chr17:21212915..21221115hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg388201
hg198201
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476222
Samples
Known GenesMAP2K3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886018
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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