A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945772



Internal ID18245937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12079536..12081203hg38UCSC Ensembl
Innerchr1:12139593..12141260hg19UCSC Ensembl
Innerchr1:12062180..12063847hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381668
hg191668
hg181668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1753079, nssv1753084, nssv1753085, nssv1753081, nssv1753080, nssv1753082, nssv1753077, nssv1753086, nssv1753078, nssv1753083
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTNFRSF8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945772
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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