A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634744



Internal ID21583049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173287821..173287821hg38UCSC Ensembl
chr4:174208972..174208972hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123960
SamplesHG00733
Known GenesGALNT7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634744
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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