A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026252



Internal ID19115469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35534827..35597022hg38UCSC Ensembl
Innerchr6:35502604..35564799hg19UCSC Ensembl
Innerchr6:35610582..35672777hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3862196
hg1962196
hg1862196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5957n100
Supporting Variantsnssv3657390, nssv3657382, nssv3657387, nssv3657385, nssv3657383, nssv3657386, nssv3657384, nssv3657389, nssv3657388
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)nsv1026252
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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