A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977754



Internal ID18612960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:88960208..88974503hg38UCSC Ensembl
Innerchr15:89503439..89517734hg19UCSC Ensembl
Innerchr15:87304443..87318738hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3814296
hg1914296
hg1814296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2036694, nssv2036692, nssv2036698, nssv2036695, nssv2036691, nssv2036696, nssv2036693, nssv2036690, nssv2036697, nssv2036699
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)nsv977754
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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