A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391036



Internal ID21379615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60113299..60113348hg38UCSC Ensembl
chr1:60578971..60579020hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15707049
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391036
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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