A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930725



Internal ID21350794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26109437..26109437hg38UCSC Ensembl
chr4:26111059..26111059hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190646
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930725
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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