A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977274



Internal ID18612480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100537842..100541678hg38UCSC Ensembl
Innerchr13:101190096..101193932hg19UCSC Ensembl
Innerchr13:99988097..99991933hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg383837
hg193837
hg183837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1973615, nssv1973606, nssv1973612, nssv1973610, nssv1973611, nssv1973608, nssv1973607, nssv1973614, nssv1973609, nssv1973613
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGGACT
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977274
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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