A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455307



Internal ID22513184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6982996..6985807hg38UCSC Ensembl
chr11:7004227..7007038hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382812
hg192812
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861425
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455307
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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