A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965157



Internal ID18253705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37134740..37136849hg38UCSC Ensembl
Innerchr3:37176231..37178340hg19UCSC Ensembl
Innerchr3:37151235..37153344hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382110
hg192110
hg182110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2278726, nssv2278734, nssv2278730, nssv2278727, nssv2278732, nssv2278728, nssv2278731, nssv2278733, nssv2278725, nssv2278729
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLRRFIP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965157
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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