A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948071



Internal ID18248231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74370569..74372427hg38UCSC Ensembl
Innerchr10:76130327..76132185hg19UCSC Ensembl
Innerchr10:75800333..75802191hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381859
hg191859
hg181859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1858235, nssv1858244, nssv1858236, nssv1858242, nssv1858240, nssv1858241, nssv1858243, nssv1858237, nssv1858239, nssv1858238
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesADK
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948071
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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