A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945877



Internal ID18592727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35121930..35122932hg38UCSC Ensembl
Innerchr1:35587531..35588533hg19UCSC Ensembl
Innerchr1:35360118..35361120hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381003
hg191003
hg181003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1758853, nssv1758848, nssv1758851, nssv1758844, nssv1758845, nssv1758847, nssv1758846, nssv1758852, nssv1758850, nssv1758849
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)nsv945877
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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