A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700663



Internal ID21222498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172368454..172368667hg38UCSC Ensembl
chr5:171795458..171795671hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811574
Supporting Variants
Samples
Known GenesSH3PXD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700663
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.578125


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