A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624578



Internal ID21572883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1603968..1603968hg38UCSC Ensembl
chr5:1604083..1604083hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134474
SamplesHG00731
Known GenesLOC728613
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624578
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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