A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650320



Internal ID18601915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180953191..181044823hg38UCSC Ensembl
Innerchr5:180380191..180471823hg19UCSC Ensembl
Innerchr5:180312797..180404429hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3891633
hg1991633
hg1891633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015914
Supporting Variants
Samples
Known GenesBTNL3, BTNL9, MIR8089
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3650320
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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