A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982511



Internal ID18617706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64405128..64406715hg38UCSC Ensembl
Innerchr9:69417546..69419133hg19UCSC Ensembl
Innerchr9:68707366..68708953hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381588
hg191588
hg181588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2744872, nssv2744795, nssv2744797, nssv2744865, nssv2744803, nssv2744802, nssv2744873, nssv2744801, nssv2744870, nssv2744799, nssv2744868, nssv2744796, nssv2744798, nssv2744866, nssv2744800, nssv2744874, nssv2744871, nssv2744804, nssv2744869, nssv2744867
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982511
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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