A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945937



Internal ID18592787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:50399014..50412606hg38UCSC Ensembl
Innerchr1:50864686..50878278hg19UCSC Ensembl
Innerchr1:50637273..50650865hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3813593
hg1913593
hg1813593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1767060, nssv1767062, nssv1767059, nssv1767056, nssv1767057, nssv1767064, nssv1767058, nssv1767065, nssv1767061, nssv1767063
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)nsv945937
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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