A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390919



Internal ID21382054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30997887..30997966hg38UCSC Ensembl
chr1:31470734..31470813hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705959
Samples
Known GenesPUM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390919
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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