A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354567



Internal ID22580236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72524376..72535660hg38UCSC Ensembl
chr11:72235420..72246704hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3811285
hg1911285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354567
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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