A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021675



Internal ID19110893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35534827..35601504hg38UCSC Ensembl
Innerchr6:35502604..35569281hg19UCSC Ensembl
Innerchr6:35610582..35677259hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3866678
hg1966678
hg1866678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5957n100
Supporting Variantsnssv3657394, nssv3657393
Samples
Known GenesFKBP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021675
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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