A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968624



Internal ID18603852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60956656..60977549hg38UCSC Ensembl
Innerchr9:39927140..39948046hg19UCSC Ensembl
Innerchr9:39917140..39938046hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3820894
hg1920907
hg1820907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2531897, nssv2531899, nssv2531892, nssv2531894, nssv2531891, nssv2531898, nssv2531896, nssv2531890, nssv2531895, nssv2531893
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968624
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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