A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469264



Internal ID22527155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75754568..75756988hg38UCSC Ensembl
chr11:75465613..75468033hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862129
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469264
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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