A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926287



Internal ID21346359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81132103..81132103hg38UCSC Ensembl
chr7:80761419..80761419hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203880
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926287
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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