A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951701



Internal ID21371771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40612215..40612864hg38UCSC Ensembl
chr8:40469734..40470383hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199564
SamplesHG002
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951701
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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