A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947784



Internal ID18594631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26935691..26946921hg38UCSC Ensembl
Innerchr10:27224620..27235850hg19UCSC Ensembl
Innerchr10:27264626..27275856hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3811231
hg1911231
hg1811231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1836418, nssv1836421, nssv1836419, nssv1836414, nssv1836423, nssv1836422, nssv1836420, nssv1836415, nssv1836416, nssv1836417
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00202-1
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947784
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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