A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972420



Internal ID18260950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92803763..92826683hg38UCSC Ensembl
Innerchr9:95566045..95588965hg19UCSC Ensembl
Innerchr9:94605866..94628786hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3822921
hg1922921
hg1822921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559895, nssv2559896, nssv2559897, nssv2559893, nssv2559894, nssv2559891, nssv2559892, nssv2559898, nssv2559900, nssv2559899
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD19P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972420
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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