A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463790



Internal ID22521675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126066369..126068980hg38UCSC Ensembl
chr11:125936264..125938875hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382612
hg192612
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463790
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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