A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971990



Internal ID18260520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18132374..18143365hg38UCSC Ensembl
Innerchr11:18153921..18164912hg19UCSC Ensembl
Innerchr11:18110497..18121488hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810992
hg1910992
hg1810992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1876974, nssv1876971, nssv1876969, nssv1876975, nssv1876972, nssv1876973, nssv1876967, nssv1876968, nssv1876970, nssv1876966
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMRGPRX3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971990
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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