A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287020



Internal ID20496238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2694497..2694497hg38UCSC Ensembl
chr6:2694731..2694731hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754983
Supporting Variants
Samples
Known GenesMYLK4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287020
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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