A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966243



Internal ID18601473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10001..24028hg38UCSC Ensembl
Innerchr4:10001..24028hg19UCSC Ensembl
Innerchr4:1..14028hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3814028
hg1914028
hg1814028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2691754, nssv2691758, nssv2691755, nssv2691753, nssv2691750, nssv2691756, nssv2691751, nssv2691752, nssv2691749, nssv2691757
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966243
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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