A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968715



Internal ID18257257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87711963..87714211hg38UCSC Ensembl
Innerchr9:90326878..90329126hg19UCSC Ensembl
Innerchr9:89516698..89518946hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382249
hg192249
hg182249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2556513, nssv2556511, nssv2556512, nssv2556515, nssv2556516, nssv2556520, nssv2556518, nssv2556519, nssv2556517, nssv2556514
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)nsv968715
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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