A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364799



Internal ID22590468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67335265..67338380hg38UCSC Ensembl
chr11:67102736..67105851hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383116
hg193116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926472
Supporting Variants
Samples
Known GenesLOC100130987
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364799
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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