A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972750



Internal ID18607966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65254059..65284640hg38UCSC Ensembl
Innerchr9:70147665..70178246hg19UCSC Ensembl
Innerchr9:69437485..69468066hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3830582
hg1930582
hg1830582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2549846, nssv2549843, nssv2549839, nssv2549841, nssv2549837, nssv2549840, nssv2549842, nssv2549844, nssv2549845, nssv2549838
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFOXD4L5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972750
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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