A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972313



Internal ID18607529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37046428..37049321hg38UCSC Ensembl
Innerchr9:37046425..37049318hg19UCSC Ensembl
Innerchr9:37036425..37039318hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg382894
hg192894
hg182894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2529438, nssv2529434, nssv2529436, nssv2529432, nssv2529441, nssv2529433, nssv2529439, nssv2529440, nssv2529435, nssv2529437
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)nsv972313
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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