A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295500



Internal ID20504718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26300923..26301167hg38UCSC Ensembl
chr11:26322470..26322714hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295500
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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