A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034786



Internal ID18777319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35508785..35597022hg38UCSC Ensembl
Innerchr6:35476562..35564799hg19UCSC Ensembl
Innerchr6:35584540..35672777hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3888238
hg1988238
hg1888238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5956n100
Supporting Variantsnssv3657378, nssv3657376, nssv3657377
Samples
Known GenesFKBP5, TULP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034786
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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