A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969544



Internal ID18604771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40236513..40240737hg38UCSC Ensembl
Innerchr9:42381531..42385755hg19UCSC Ensembl
Innerchr9:42371527..42375751hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384225
hg194225
hg184225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727240, nssv2728092, nssv2728095, nssv2728090, nssv2728036, nssv2728093, nssv2728087, nssv2727239, nssv2727242, nssv2727243, nssv2728088, nssv2727238, nssv2728037, nssv2728094, nssv2728086, nssv2727241, nssv2727236, nssv2727237, nssv2728091, nssv2728089
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969544
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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