A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435392



Internal ID21397394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127936059..127947705hg38UCSC Ensembl
chr8:128948305..128959951hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3811647
hg1911647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15745724
SamplesNB08
Known GenesPVT1, TMEM75
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435392
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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