A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945989



Internal ID18592839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:68374805..68375626hg38UCSC Ensembl
Innerchr1:68840488..68841309hg19UCSC Ensembl
Innerchr1:68613076..68613897hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38822
hg19822
hg18822
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1770359, nssv1770362, nssv1770358, nssv1770356, nssv1770360, nssv1770364, nssv1770363, nssv1770357, nssv1770361, nssv1770355
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)nsv945989
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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