A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546762



Internal ID21871117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78366199..78366332hg38UCSC Ensembl
chr5:77662023..77662156hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017438
Supporting Variants
Samples
Known GenesSCAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546762
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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