A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968701



Internal ID18603929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66181347..66202614hg38UCSC Ensembl
Innerchr9:70713856..70735249hg19UCSC Ensembl
Innerchr9:69953676..69975069hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3821268
hg1921394
hg1821394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2551010, nssv2551007, nssv2551014, nssv2551009, nssv2551008, nssv2551011, nssv2551012, nssv2551013, nssv2551015, nssv2551006
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)nsv968701
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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