A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151943



Internal ID21443817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40612215..40612863hg38UCSC Ensembl
chr8:40469734..40470382hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581977
Supporting Variants
SamplesHG00732
Known GenesZMAT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151943
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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