A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984089



Internal ID18272593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72058465..72059833hg38UCSC Ensembl
Innerchr15:72350806..72352174hg19UCSC Ensembl
Innerchr15:70137860..70139228hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381369
hg191369
hg181369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2030260, nssv2030261, nssv2030256, nssv2030255, nssv2030258, nssv2030262, nssv2030263, nssv2030254, nssv2030257, nssv2030259
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMYO9A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984089
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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