A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982366



Internal ID18270875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39118047..39119137hg38UCSC Ensembl
Innerchr9:39118044..39119134hg19UCSC Ensembl
Innerchr9:39108044..39109134hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg381091
hg191091
hg181091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2723444, nssv2723450, nssv2723452, nssv2723446, nssv2723445, nssv2723443, nssv2723448, nssv2723447, nssv2723451, nssv2723449
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCNTNAP3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982366
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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