A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026532



Internal ID19115750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35534827..35600785hg38UCSC Ensembl
Innerchr6:35502604..35568562hg19UCSC Ensembl
Innerchr6:35610582..35676540hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3865959
hg1965959
hg1865959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5957n100
Supporting Variantsnssv3657391, nssv3657392
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)nsv1026532
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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