A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627326



Internal ID21575631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78669386..78669386hg38UCSC Ensembl
chr8:79581621..79581621hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146875
SamplesNA19983
Known GenesZC2HC1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627326
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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