A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455004



Internal ID22512881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31990454..31995730hg38UCSC Ensembl
chr11:32012000..32017276hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455004
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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