A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581977



Internal ID21530484
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 StatusM
Merged Variants
Supporting Variantsnssv17151943
SamplesHG00732
Known GenesZMAT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581977
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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