A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691548



Internal ID18643143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132769940..132833582hg38UCSC Ensembl
Innerchr8:133782186..133845827hg19UCSC Ensembl
Innerchr8:133851368..133915009hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3863643
hg1963642
hg1863642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016620
Supporting Variants
Samples
Known GenesPHF20L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691548
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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