A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968647



Internal ID18603875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42637160..42653760hg38UCSC Ensembl
Innerchr9:44317359..44333959hg19UCSC Ensembl
Innerchr9:44257355..44273955hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816601
hg1916601
hg1816601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2540523, nssv2540522, nssv2540527, nssv2540524, nssv2540526, nssv2540528, nssv2540531, nssv2540530, nssv2540525, nssv2540529
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)nsv968647
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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