A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623033



Internal ID21571338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139314998..139314998hg38UCSC Ensembl
chr4:140236152..140236152hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131002, nssv17132528
SamplesHG00096, NA24385
Known GenesNAA15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623033
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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