A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961380



Internal ID18596626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11102615..11103853hg38UCSC Ensembl
Innerchr2:11242741..11243979hg19UCSC Ensembl
Innerchr2:11160192..11161430hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381239
hg191239
hg181239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2163987, nssv2163982, nssv2163984, nssv2163983, nssv2163985, nssv2163980, nssv2163981, nssv2163979, nssv2163988, nssv2163986
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFLJ33534
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961380
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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