A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968745



Internal ID18603973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107834446..107835763hg38UCSC Ensembl
Innerchr9:110596727..110598044hg19UCSC Ensembl
Innerchr9:109636548..109637865hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381318
hg191318
hg181318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561692, nssv2561697, nssv2561695, nssv2561693, nssv2561691, nssv2561696, nssv2561699, nssv2561698, nssv2561690, nssv2561694
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)nsv968745
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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