A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468438



Internal ID22526327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119634103..119639002hg38UCSC Ensembl
chr11:119504814..119509712hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384900
hg194899
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853160
Supporting Variants
Samples
Known GenesPVRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468438
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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