A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969461



Internal ID18604688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158840060..158842129hg38UCSC Ensembl
Innerchr6:159261092..159263161hg19UCSC Ensembl
Innerchr6:159181080..159183149hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382070
hg192070
hg182070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2427949, nssv2427950, nssv2427943, nssv2427941, nssv2427947, nssv2427944, nssv2427946, nssv2427945, nssv2427948, nssv2427942
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOSTCP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969461
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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