A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4004461



Internal ID22066092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378084..39541712hg38UCSC Ensembl
Outerchr8:39373140..39546375hg38UCSC Ensembl
Innerchr8:39235603..39399231hg19UCSC Ensembl
Outerchr8:39230659..39403894hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38173236
hg19173236
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154343
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4004461
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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