A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942903



Internal ID21362972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43106314..43107075hg38UCSC Ensembl
chr1:43571985..43572746hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15182827
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942903
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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