A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982213



Internal ID18617408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36012305..36014163hg38UCSC Ensembl
Innerchr9:36012302..36014160hg19UCSC Ensembl
Innerchr9:36002302..36004160hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381859
hg191859
hg181859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2528696, nssv2528694, nssv2528699, nssv2528702, nssv2528697, nssv2528700, nssv2528698, nssv2528701, nssv2528695, nssv2528703
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)nsv982213
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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