A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971972



Internal ID18607188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3890915..3893533hg38UCSC Ensembl
Innerchr11:3912145..3914763hg19UCSC Ensembl
Innerchr11:3868721..3871339hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382619
hg192619
hg182619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1871200, nssv1871202, nssv1871201, nssv1871198, nssv1871193, nssv1871199, nssv1871195, nssv1871194, nssv1871196, nssv1871197
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSTIM1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971972
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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