A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972445



Internal ID18607661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115427562..115430845hg38UCSC Ensembl
Innerchr9:118189841..118193124hg19UCSC Ensembl
Innerchr9:117229662..117232945hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383284
hg193284
hg183284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2562806, nssv2562811, nssv2562814, nssv2562808, nssv2562805, nssv2562812, nssv2562810, nssv2562813, nssv2562807, nssv2562809
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)nsv972445
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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