A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627469



Internal ID21575774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81666267..81666267hg38UCSC Ensembl
chr8:82578502..82578502hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158663
SamplesHG01596
Known GenesIMPA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627469
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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