A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947797



Internal ID18247958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28521083..28523400hg38UCSC Ensembl
Innerchr10:28810012..28812329hg19UCSC Ensembl
Innerchr10:28850018..28852335hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg382318
hg192318
hg182318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1837706, nssv1837698, nssv1837705, nssv1837704, nssv1837700, nssv1837701, nssv1837699, nssv1837697, nssv1837702, nssv1837703
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWAC-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947797
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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