A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972374



Internal ID18607590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66721645..66722800hg38UCSC Ensembl
Innerchr9:66059051..66060206hg19UCSC Ensembl
Innerchr9:65798871..65800026hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381156
hg191156
hg181156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2545879, nssv2545881, nssv2545872, nssv2545875, nssv2545874, nssv2545876, nssv2545873, nssv2545880, nssv2545877, nssv2545878
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972374
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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