A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004584



Internal ID21913927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150658472..150658760hg38UCSC Ensembl
chr6:150979608..150979896hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570248
Samples
Known GenesPLEKHG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004584
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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