A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966263



Internal ID18254807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39453957..39456830hg38UCSC Ensembl
Innerchr4:39455577..39458450hg19UCSC Ensembl
Innerchr4:39131972..39134845hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382874
hg192874
hg182874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2314321, nssv2314315, nssv2314317, nssv2314320, nssv2314314, nssv2314319, nssv2314316, nssv2314322, nssv2314323, nssv2314318
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR1273H, RPL9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966263
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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