A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965712



Internal ID18600942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34209972..34224281hg38UCSC Ensembl
Innerchr6:34177749..34192058hg19UCSC Ensembl
Innerchr6:34285727..34300036hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3814310
hg1914310
hg1814310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2405146, nssv2405145, nssv2405139, nssv2405141, nssv2405140, nssv2405143, nssv2405144, nssv2405148, nssv2405147, nssv2405142
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965712
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