A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928228



Internal ID21348297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81886660..81887002hg38UCSC Ensembl
chr5:81182479..81182821hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196349
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928228
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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