A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021841



Internal ID19111059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35537534..35594375hg38UCSC Ensembl
Innerchr6:35505311..35562152hg19UCSC Ensembl
Innerchr6:35613289..35670130hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3856842
hg1956842
hg1856842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5957n100
Supporting Variantsnssv3657405
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)nsv1021841
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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