A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951099



Internal ID22726481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93405814..93405814hg38UCSC Ensembl
chr6:94115532..94115532hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442578
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951099
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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