A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972739



Internal ID18607955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62918791..62954364hg38UCSC Ensembl
Innerchr9:66574615..66610188hg19UCSC Ensembl
Innerchr9:66314435..66350008hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3835574
hg1935574
hg1835574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2547972, nssv2547970, nssv2547973, nssv2547977, nssv2547975, nssv2547971, nssv2547976, nssv2547969, nssv2547974, nssv2547978
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)nsv972739
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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