A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15196955



Internal ID21335751
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950852
Supporting Variants
SamplesHG002
Known GenesNPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15196955
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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