A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974365



Internal ID18609576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91602027..91607032hg38UCSC Ensembl
Innerchr14:92068371..92073376hg19UCSC Ensembl
Innerchr14:91138124..91143129hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg385006
hg195006
hg185006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1995948, nssv1995946, nssv1995944, nssv1995949, nssv1995942, nssv1995947, nssv1995941, nssv1995940, nssv1995945, nssv1995943
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCATSPERB
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974365
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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