A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581704



Internal ID21773747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65367661..65385802hg38UCSC Ensembl
chr11:65135132..65153273hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3818142
hg1918142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027835
Supporting Variants
Samples
Known GenesSLC25A45
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581704
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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