A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010737



Internal ID74786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40633681..40633758hg38UCSC Ensembl
chr8:40491200..40491277hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483556
Supporting Variants
Samples
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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