A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876950



Internal ID22651913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12534375..12534768hg38UCSC Ensembl
chr1:12594414..12594806hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38394
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876950
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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