A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972069



Internal ID18607285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107396566..107404525hg38UCSC Ensembl
Innerchr11:107267292..107275251hg19UCSC Ensembl
Innerchr11:106772502..106780461hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg387960
hg197960
hg187960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1904067, nssv1904068, nssv1904061, nssv1904062, nssv1904069, nssv1904064, nssv1904065, nssv1904066, nssv1904063, nssv1904070
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCWF19L2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972069
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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