A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977239



Internal ID18612445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51159396..51164104hg38UCSC Ensembl
Innerchr13:51733532..51738240hg19UCSC Ensembl
Innerchr13:50631533..50636241hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg384709
hg194709
hg184709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1964062, nssv1962759, nssv1962757, nssv1962761, nssv1964066, nssv1962758, nssv1964065, nssv1964064, nssv1962760, nssv1964063
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00371
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977239
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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