A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945827



Internal ID18592677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23969201..23971390hg38UCSC Ensembl
Innerchr1:24295691..24297880hg19UCSC Ensembl
Innerchr1:24168278..24170467hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382190
hg192190
hg182190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765989, nssv1765996, nssv1765993, nssv1765995, nssv1765991, nssv1765992, nssv1765988, nssv1765990, nssv1765987, nssv1765994
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSRSF10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945827
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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