A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936291



Internal ID21356360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39710094..39710094hg38UCSC Ensembl
chr7:39749693..39749693hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203836
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936291
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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