A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654020



Internal ID15390672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35537534..35639794hg38UCSC Ensembl
Innerchr6:35505311..35607571hg19UCSC Ensembl
Innerchr6:35613289..35715549hg18UCSC Ensembl
Innerchr6:35613289..35715549hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38102261
hg19102261
hg18102261
hg17102261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517211
Supporting Variants
Samples
Known GenesFKBP5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654020
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer