A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945699



Internal ID18592550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22118..35020hg38UCSC Ensembl
Innerchr1:22118..35020hg19UCSC Ensembl
Innerchr1:11981..24883hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3812903
hg1912903
hg1812903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1749206, nssv1749211, nssv1749207, nssv1749209, nssv1749215, nssv1749214, nssv1749213, nssv1749205, nssv1749208, nssv1749210
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM138A, FAM138F, WASH7P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945699
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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