A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983030



Internal ID18271538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61636758..61639129hg38UCSC Ensembl
Innerchr11:61404230..61406601hg19UCSC Ensembl
Innerchr11:61160806..61163177hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382372
hg192372
hg182372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1891630, nssv1891631, nssv1891629, nssv1891622, nssv1891624, nssv1891625, nssv1891628, nssv1891623, nssv1891626, nssv1891627
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPLP0P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983030
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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