A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948066



Internal ID18594912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73242870..73243833hg38UCSC Ensembl
Innerchr10:75002628..75003591hg19UCSC Ensembl
Innerchr10:74672634..74673597hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1858549, nssv1856981, nssv1858550, nssv1856983, nssv1858553, nssv1858552, nssv1858551, nssv1856980, nssv1856982, nssv1856984
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDNAJC9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948066
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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