A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950431



Internal ID21370500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23549706..23550346hg38UCSC Ensembl
chr8:23407219..23407859hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15198803
SamplesHG002
Known GenesSLC25A37
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950431
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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