A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942696



Internal ID21362765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107368450..107368850hg38UCSC Ensembl
chr8:108380678..108381078hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198871
SamplesHG002
Known GenesANGPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942696
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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