A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950852



Internal ID21370921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171403994..171404253hg38UCSC Ensembl
chr5:170830998..170831257hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196955
SamplesHG002
Known GenesNPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950852
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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