A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389497



Internal ID21380632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91055627..91055947hg38UCSC Ensembl
chr10:92815384..92815704hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704932
Samples
Known GenesLINC00502
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389497
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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