A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939354



Internal ID21359423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192857700..192857700hg38UCSC Ensembl
chr1:192826830..192826830hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189043
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939354
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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