A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007991



Internal ID21917334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152251666..152251735hg38UCSC Ensembl
chr6:152572801..152572870hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569138
Samples
Known GenesSYNE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007991
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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