A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935088



Internal ID21355158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38530451..38530451hg38UCSC Ensembl
chr1:38996123..38996123hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15192479
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935088
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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