A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571305



Internal ID21763348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172368476..172368686hg38UCSC Ensembl
chr5:171795480..171795690hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015515
Supporting Variants
Samples
Known GenesSH3PXD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571305
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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