A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548019



Internal ID21872374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78392026..78392077hg38UCSC Ensembl
chr5:77687850..77687901hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013758
Supporting Variants
Samples
Known GenesSCAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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