A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965777



Internal ID18601007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144199032..144201389hg38UCSC Ensembl
Innerchr6:144520169..144522526hg19UCSC Ensembl
Innerchr6:144561862..144564219hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382358
hg192358
hg182358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2425737, nssv2425734, nssv2425738, nssv2425735, nssv2425740, nssv2425731, nssv2425732, nssv2425736, nssv2425739, nssv2425733
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)nsv965777
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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