A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967035



Internal ID18602264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:88188733..88189818hg38UCSC Ensembl
Innerchr3:88237883..88238968hg19UCSC Ensembl
Innerchr3:88320573..88321658hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg381086
hg191086
hg181086
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2287669, nssv2287668, nssv2287672, nssv2287670, nssv2287676, nssv2287677, nssv2287674, nssv2287675, nssv2287673, nssv2287671
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967035
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer