A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704392



Internal ID21376668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37770691..37770824hg38UCSC Ensembl
chr8:37628209..37628342hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388791
Supporting Variants
Samples
Known GenesPROSC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704392
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0258621


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer