A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749210



Internal ID21389182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173545913..173547747hg38UCSC Ensembl
chr5:172972916..172974750hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381835
hg191835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434565
Supporting Variants
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749210
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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