A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026900



Internal ID18769431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180951876..181018344hg38UCSC Ensembl
Innerchr5:180378876..180445344hg19UCSC Ensembl
Innerchr5:180311482..180377950hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3866469
hg1966469
hg1866469
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5853n100
Supporting Variantsnssv3650302, nssv3650303, nssv3650305, nssv3650304
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)nsv1026900
Frequency
Sample Size29084
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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