A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961898



Internal ID18597144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:155083275..155089775hg38UCSC Ensembl
Innerchr2:155939787..155946287hg19UCSC Ensembl
Innerchr2:155648033..155654533hg18UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg386501
hg196501
hg186501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2208122, nssv2208123, nssv2208121, nssv2208120, nssv2208124, nssv2208119, nssv2208118, nssv2208125, nssv2208117, nssv2208116
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961898
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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