A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351818



Internal ID22577487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64203622..64204052hg38UCSC Ensembl
chr11:63971094..63971524hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918368
Supporting Variants
Samples
Known GenesSTIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351818
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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