A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972770



Internal ID18607986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86264364..86266396hg38UCSC Ensembl
Innerchr9:88879279..88881311hg19UCSC Ensembl
Innerchr9:88069099..88071131hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382033
hg192033
hg182033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555143, nssv2555142, nssv2555139, nssv2555141, nssv2555146, nssv2555137, nssv2555140, nssv2555144, nssv2555145, nssv2555138
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesISCA1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972770
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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