A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864030



Internal ID22638965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66389716..66390715hg38UCSC Ensembl
chr15:66682054..66683053hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473544, nssv17471753
Samples
Known GenesMAP2K1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864030
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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