A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025286



Internal ID18767818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180951876..181061260hg38UCSC Ensembl
Innerchr5:180378876..180488260hg19UCSC Ensembl
Innerchr5:180311482..180420866hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38109385
hg19109385
hg18109385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5855n100
Supporting Variantsnssv3746747, nssv3650310
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)nsv1025286
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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