A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464513



Internal ID22522400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3364747..3392779hg38UCSC Ensembl
chr11:3385977..3414009hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828033
hg1928033
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858857
Supporting Variants
Samples
Known GenesLOC650368, OR7E12P, ZNF195
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464513
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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