A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971988



Internal ID18607204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17046815..17063431hg38UCSC Ensembl
Innerchr11:17068362..17084978hg19UCSC Ensembl
Innerchr11:17024938..17041554hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3816617
hg1916617
hg1816617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1878062, nssv1878058, nssv1878060, nssv1878057, nssv1878063, nssv1878054, nssv1878055, nssv1878061, nssv1878056, nssv1878059
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7E14P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971988
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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