A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591191



Internal ID21783234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64334123..64336156hg38UCSC Ensembl
chr11:64101595..64103628hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591191
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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