A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945754



Internal ID18592605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5848989..5850865hg38UCSC Ensembl
Innerchr1:5909049..5910925hg19UCSC Ensembl
Innerchr1:5831636..5833512hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381877
hg191877
hg181877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1751366, nssv1751363, nssv1751364, nssv1751367, nssv1751368, nssv1751371, nssv1751365, nssv1751362, nssv1751370, nssv1751369
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)nsv945754
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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