A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936853



Internal ID21356922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73588490..73588490hg38UCSC Ensembl
chr7:73002820..73002820hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203634
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936853
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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