A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036143



Internal ID21945486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64271059..64271320hg38UCSC Ensembl
chr11:64038531..64038792hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578334
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036143
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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