A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431305



Internal ID21393307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33013272..33049225hg38UCSC Ensembl
chr10:33302200..33338153hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3835954
hg1935954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749382
SamplesSMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431305
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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