A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951870



Internal ID21371939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152674710..152674710hg38UCSC Ensembl
chr7:152371795..152371795hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203726
SamplesHG002
Known GenesXRCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951870
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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