A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631174



Internal ID21579479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34974861..34974861hg38UCSC Ensembl
chr7:35014473..35014473hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152838
SamplesNA18939
Known GenesDPY19L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631174
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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