A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982301



Internal ID18617496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68238951..68282900hg38UCSC Ensembl
Innerchr9:70853867..70897816hg19UCSC Ensembl
Innerchr9:70043687..70087636hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3843950
hg1943950
hg1843950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2551077, nssv2551076, nssv2551075, nssv2551081, nssv2551079, nssv2551083, nssv2551084, nssv2551082, nssv2551078, nssv2551080
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD3, CBWD5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982301
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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