A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158372



Internal ID21426919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78687702..78687771hg38UCSC Ensembl
chr8:79599937..79600006hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567444
Supporting Variants
SamplesHG00731
Known GenesZC2HC1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158372
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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