A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941302



Internal ID21361371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8912172..8912172hg38UCSC Ensembl
chr1:8972231..8972231hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192045, nssv15192044
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941302
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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