A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023887



Internal ID21933230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64798559..64798694hg38UCSC Ensembl
chr11:64566031..64566166hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588286
Samples
Known GenesMAP4K2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023887
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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