A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028752



Internal ID19117970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168320807..168362639hg38UCSC Ensembl
Innerchr6:168721487..168763319hg19UCSC Ensembl
Innerchr6:168464336..168506168hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3841833
hg1941833
hg1841833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653071
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028752
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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