A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626661



Internal ID21574966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60614220..60614220hg38UCSC Ensembl
chr8:61526779..61526779hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149014
SamplesHG00731
Known GenesRAB2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626661
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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