A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971991



Internal ID18607207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18168150..18178928hg38UCSC Ensembl
Innerchr11:18189697..18200475hg19UCSC Ensembl
Innerchr11:18146273..18157051hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810779
hg1910779
hg1810779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877856, nssv1877861, nssv1877860, nssv1877859, nssv1877862, nssv1877863, nssv1877855, nssv1877857, nssv1877864, nssv1877858
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMRGPRX4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971991
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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