A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431396



Internal ID21393398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8482889..8483322hg38UCSC Ensembl
chr10:8524852..8525285hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750084
SamplesSMI034
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431396
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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