A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431380



Internal ID21393382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7572795..7573673hg38UCSC Ensembl
chr10:7614758..7615636hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754072
SamplesMDQ025
Known GenesITIH5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431380
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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