A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467397



Internal ID22525288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38498469..38499500hg38UCSC Ensembl
chr11:38520019..38521050hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381032
hg191032
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467397
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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