A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973634



Internal ID18608849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42857533..42869601hg38UCSC Ensembl
Innerchr9:44101518..44113586hg19UCSC Ensembl
Innerchr9:44041514..44053582hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3812069
hg1912069
hg1812069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2735415, nssv2735413, nssv2735388, nssv2735385, nssv2735421, nssv2735416, nssv2735380, nssv2735383, nssv2735419, nssv2735389, nssv2735386, nssv2735420, nssv2735418, nssv2735381, nssv2735414, nssv2735422, nssv2735382, nssv2735384, nssv2735417, nssv2735387
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973634
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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