A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079321



Internal ID21988554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10903227..10903227hg38UCSC Ensembl
chr6:10903460..10903460hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558814
Samples
Known GenesSYCP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079321
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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