A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947882



Internal ID21367951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2960889..2960958hg38UCSC Ensembl
chr4:2962616..2962685hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180145
SamplesHG002
Known GenesNOP14
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947882
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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