A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354849



Internal ID22580518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73960434..73960573hg38UCSC Ensembl
chr11:73671479..73671618hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908338
Supporting Variants
Samples
Known GenesDNAJB13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354849
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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