A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963386



Internal ID18598627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182460656..182467026hg38UCSC Ensembl
Innerchr3:182178444..182184814hg19UCSC Ensembl
Innerchr3:183661138..183667508hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg386371
hg196371
hg186371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2303253, nssv2303247, nssv2303256, nssv2303249, nssv2303252, nssv2303254, nssv2303248, nssv2303251, nssv2303255, nssv2303250
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFLJ46066
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963386
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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