A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972645



Internal ID18607861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5776519..5784037hg38UCSC Ensembl
Innerchr9:5776519..5784037hg19UCSC Ensembl
Innerchr9:5766519..5774037hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg387519
hg197519
hg187519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2521839, nssv2521841, nssv2521835, nssv2521840, nssv2521842, nssv2521837, nssv2521843, nssv2521836, nssv2521844, nssv2521838
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKIAA1432
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972645
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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