A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018795



Internal ID21928138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36446094..36446209hg38UCSC Ensembl
chr6:36413871..36413986hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563747
Samples
Known GenesKCTD20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018795
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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