A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625248



Internal ID21817295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11880054..11880366hg38UCSC Ensembl
chr18:11880053..11880365hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027239
Supporting Variants
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625248
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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