A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670258



Internal ID15406910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35537534..35594863hg38UCSC Ensembl
Innerchr6:35505311..35562640hg19UCSC Ensembl
Innerchr6:35613289..35670618hg18UCSC Ensembl
Innerchr6:35613289..35670618hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3857330
hg1957330
hg1857330
hg1757330
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)nssv670258
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