A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961860



Internal ID18250420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:110096240..110101376hg38UCSC Ensembl
Innerchr2:110853817..110858953hg19UCSC Ensembl
Innerchr2:110211106..110216242hg18UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg385137
hg195137
hg185137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2194866, nssv2194862, nssv2194864, nssv2194869, nssv2194868, nssv2194871, nssv2194865, nssv2194867, nssv2194863, nssv2194870
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMALL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961860
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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