A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937771



Internal ID21357841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223031357..223031436hg38UCSC Ensembl
chr1:223204699..223204778hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180447
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937771
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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