A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469263



Internal ID22527154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39598138..39604935hg38UCSC Ensembl
chr11:39619688..39626485hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386798
hg196798
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469263
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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