A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977742



Internal ID18612948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79236253..79238263hg38UCSC Ensembl
Innerchr15:79528595..79530605hg19UCSC Ensembl
Innerchr15:77315650..77317660hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382011
hg192011
hg182011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2033691, nssv2033687, nssv2033690, nssv2033692, nssv2033688, nssv2033684, nssv2033685, nssv2033686, nssv2033693, nssv2033689
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC729911
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977742
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