A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032715



Internal ID18775249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180951876..181018209hg38UCSC Ensembl
Innerchr5:180378876..180445209hg19UCSC Ensembl
Innerchr5:180311482..180377815hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3866334
hg1966334
hg1866334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5854n100
Supporting Variantsnssv3650301
Samples
Known GenesBTNL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032715
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