A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007458



Internal ID21916801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168074428..168075072hg38UCSC Ensembl
chr6:168475108..168475752hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575523
Samples
Known GenesFRMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007458
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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