A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467999



Internal ID22525888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95261480..95263725hg38UCSC Ensembl
chr11:94994644..94996889hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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