A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045605



Internal ID98168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32587144..32588591hg38UCSC Ensembl
chr11:32608690..32610137hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381448
hg191448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143029
Supporting Variants
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045605
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002189


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