A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465350



Internal ID22523239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34442790..34444689hg38UCSC Ensembl
chr11:34464337..34466236hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861519
Supporting Variants
Samples
Known GenesCAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465350
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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