A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984108



Internal ID18272612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90630685..90638800hg38UCSC Ensembl
Innerchr15:91173917..91182032hg19UCSC Ensembl
Innerchr15:88974921..88983036hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg388116
hg198116
hg188116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2038495, nssv2038504, nssv2038497, nssv2038496, nssv2038500, nssv2038502, nssv2038501, nssv2038498, nssv2038499, nssv2038503
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCRTC3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984108
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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