A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970181



Internal ID18605405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156976433..156978741hg38UCSC Ensembl
Innerchr6:157297567..157299875hg19UCSC Ensembl
Innerchr6:157339259..157341567hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382309
hg192309
hg182309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2426957, nssv2426955, nssv2426959, nssv2426963, nssv2426962, nssv2426958, nssv2426956, nssv2426961, nssv2426954, nssv2426960
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesARID1B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970181
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