A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368243



Internal ID22593912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15017487..15022150hg38UCSC Ensembl
chr11:15039033..15043696hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384664
hg194664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368243
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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