A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925701



Internal ID21345775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791141..15791544hg38UCSC Ensembl
chr4:15792764..15793167hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180066
SamplesHG002
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925701
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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