A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968661



Internal ID18257203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67670061..67721653hg38UCSC Ensembl
Innerchr9:46335906..46389835hg19UCSC Ensembl
Innerchr9:46225902..46279831hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3851593
hg1953930
hg1853930
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2542865, nssv2542867, nssv2542860, nssv2542862, nssv2542868, nssv2542863, nssv2542861, nssv2542864, nssv2542869, nssv2542866
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM27E1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968661
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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