A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947792



Internal ID18247953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27904140..27907619hg38UCSC Ensembl
Innerchr10:28193069..28196548hg19UCSC Ensembl
Innerchr10:28233075..28236554hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383480
hg193480
hg183480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1835981, nssv1835974, nssv1835980, nssv1835977, nssv1835975, nssv1835978, nssv1835979, nssv1835976, nssv1835973, nssv1835972
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesARMC4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947792
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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