A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933394



Internal ID21353463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169761276..169761583hg38UCSC Ensembl
chr1:169730417..169730724hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177140
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933394
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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