A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632630



Internal ID21580935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34967726..34967726hg38UCSC Ensembl
chr7:35007338..35007338hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150740
SamplesHG02011
Known GenesDPY19L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632630
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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