A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007192



Internal ID21916535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151450493..151450592hg38UCSC Ensembl
chr6:151771628..151771727hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561973
Samples
Known GenesRMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007192
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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