A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945760



Internal ID18592611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8748916..8751645hg38UCSC Ensembl
Innerchr1:8808975..8811704hg19UCSC Ensembl
Innerchr1:8731562..8734291hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382730
hg192730
hg182730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1752615, nssv1752610, nssv1752616, nssv1752608, nssv1752612, nssv1752614, nssv1752611, nssv1752609, nssv1752613, nssv1752607
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRERE
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945760
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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