A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751197



Internal ID21391489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122955083..122955839hg38UCSC Ensembl
chr8:123967323..123968079hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435389
Supporting Variants
SamplesSMI018
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751197
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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