A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030863



Internal ID18773394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26370778..26405762hg38UCSC Ensembl
Innerchr6:26371006..26405990hg19UCSC Ensembl
Innerchr6:26478985..26513969hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3834985
hg1934985
hg1834985
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654845, nssv3654844
Samples
Known GenesBTN2A2, BTN3A1, BTN3A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030863
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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