A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967079



Internal ID18255622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154351976..154353242hg38UCSC Ensembl
Innerchr3:154069765..154071031hg19UCSC Ensembl
Innerchr3:155552459..155553725hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381267
hg191267
hg181267
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2300727, nssv2300732, nssv2300726, nssv2300730, nssv2300728, nssv2300724, nssv2300723, nssv2300725, nssv2300731, nssv2300729
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGPR149
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967079
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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