A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367590



Internal ID22593259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64194620..64195643hg38UCSC Ensembl
chr11:63962092..63963115hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381024
hg191024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916655
Supporting Variants
Samples
Known GenesSTIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367590
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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