A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356844



Internal ID22582513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19512472..19512546hg38UCSC Ensembl
chr11:19534019..19534093hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913094
Supporting Variants
Samples
Known GenesNAV2, NAV2-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356844
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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