A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945837



Internal ID18592687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25402866..25425831hg38UCSC Ensembl
Innerchr1:25729357..25752322hg19UCSC Ensembl
Innerchr1:25601944..25624909hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3822966
hg1922966
hg1822966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765947, nssv1765942, nssv1765946, nssv1765948, nssv1765945, nssv1765940, nssv1765941, nssv1765944, nssv1765943, nssv1765949
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRHCE
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945837
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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