A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030735



Internal ID21940078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34160620..34160741hg38UCSC Ensembl
chr11:34182167..34182288hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587875
Samples
Known GenesABTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030735
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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