A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946402



Internal ID21366472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100572269..100572371hg38UCSC Ensembl
chr4:101493426..101493528hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196476
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946402
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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