A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017605



Internal ID19106822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86238415..86326882hg38UCSC Ensembl
Innerchr6:86948133..87036600hg19UCSC Ensembl
Innerchr6:87004852..87093319hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3888468
hg1988468
hg1888468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648906
Samples
Known GenesMIR548AD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017605
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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