A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927429



Internal ID21347498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75962621..75962695hg38UCSC Ensembl
chr1:76428306..76428380hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183396
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927429
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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