A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745724



Internal ID21388498
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 StatusS
Merged Variantsnsv4435392
Supporting Variants
SamplesNB08
Known GenesPVT1, TMEM75
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745724
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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