A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947961



Internal ID18594807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47463363..47483046hg38UCSC Ensembl
Innerchr10:48256316..48275999hg19UCSC Ensembl
Innerchr10:47876322..47896005hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3819684
hg1919684
hg1819684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1856689, nssv1856693, nssv1856687, nssv1856692, nssv1856691, nssv1856690, nssv1856686, nssv1856684, nssv1856685, nssv1856688
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANXA8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947961
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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