A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689717



Internal ID18641312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91112535..91173829hg38UCSC Ensembl
Innerchr8:92124763..92186057hg19UCSC Ensembl
Innerchr8:92193939..92255233hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3861295
hg1961295
hg1861295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028288
Supporting Variants
Samples
Known GenesLRRC69
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689717
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