A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389767



Internal ID21380902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75869953..75870289hg38UCSC Ensembl
chr2:76097079..76097415hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706682
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389767
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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