A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928157



Internal ID21348226
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 StatusM
Merged Variants
Supporting Variantsnssv15196958
SamplesHG002
Known GenesSH3PXD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928157
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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