A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038735



Internal ID21948078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66387120..66392528hg38UCSC Ensembl
chr11:66154591..66159999hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385409
hg195409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038735
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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