A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945962



Internal ID18246126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55222668..55229122hg38UCSC Ensembl
Innerchr1:55688341..55694795hg19UCSC Ensembl
Innerchr1:55460929..55467383hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg386455
hg196455
hg186455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1766976, nssv1766975, nssv1766982, nssv1766980, nssv1766981, nssv1766974, nssv1766978, nssv1766979, nssv1766977, nssv1766973
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR4422
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945962
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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