A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019593



Internal ID19108811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35537534..35611598hg38UCSC Ensembl
Innerchr6:35505311..35579375hg19UCSC Ensembl
Innerchr6:35613289..35687353hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3874065
hg1974065
hg1874065
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5957n100
Supporting Variantsnssv3657417
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)nsv1019593
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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