A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974589



Internal ID18609800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66371445..66383000hg38UCSC Ensembl
Innerchr15:66663783..66675338hg19UCSC Ensembl
Innerchr15:64450837..64462392hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3811556
hg1911556
hg1811556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028944, nssv2028949, nssv2028951, nssv2028945, nssv2028952, nssv2028947, nssv2028953, nssv2028948, nssv2028946, nssv2028950
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974589
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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