A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350638



Internal ID22576307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10660124..10660525hg38UCSC Ensembl
chr11:10681671..10682072hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926361
Supporting Variants
Samples
Known GenesMRVI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350638
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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