A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018140



Internal ID21927483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11604808..11604865hg38UCSC Ensembl
chr6:11605041..11605098hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018140
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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