A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581177



Internal ID21773220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19209925..19213692hg38UCSC Ensembl
chr11:19231472..19235239hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383768
hg193768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030212
Supporting Variants
Samples
Known GenesCSRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581177
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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