A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976134



Internal ID18611341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:74377716..74379002hg38UCSC Ensembl
Innerchr13:74951853..74953139hg19UCSC Ensembl
Innerchr13:73849854..73851140hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381287
hg191287
hg181287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1969100, nssv1969097, nssv1969096, nssv1969098, nssv1969099, nssv1969103, nssv1969102, nssv1969101, nssv1969104, nssv1969105
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976134
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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