A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975889



Internal ID18611096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18904615..18973672hg38UCSC Ensembl
Innerchr11:18926162..18995219hg19UCSC Ensembl
Innerchr11:18882738..18951795hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3869058
hg1969058
hg1869058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1878549, nssv1878546, nssv1878553, nssv1878289, nssv1878552, nssv1878548, nssv1878547, nssv1878550, nssv1878551, nssv1878545
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMRGPRX1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975889
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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