A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975138



Internal ID18263660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1883941..1892547hg38UCSC Ensembl
Innerchr11:1905171..1913777hg19UCSC Ensembl
Innerchr11:1861747..1870353hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388607
hg198607
hg188607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1871579, nssv1871576, nssv1871582, nssv1871581, nssv1871575, nssv1871577, nssv1871583, nssv1871574, nssv1871578, nssv1871580
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLSP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975138
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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