A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947822



Internal ID18594669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32229115..32242846hg38UCSC Ensembl
Innerchr10:32518043..32531774hg19UCSC Ensembl
Innerchr10:32558049..32571780hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3813732
hg1913732
hg1813732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1838135, nssv1838138, nssv1838141, nssv1838140, nssv1838134, nssv1838139, nssv1838142, nssv1838137, nssv1838143, nssv1838136
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)nsv947822
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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