A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949879



Internal ID21369949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26163321..26163647hg38UCSC Ensembl
chr1:26489812..26490138hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181998
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949879
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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