A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961038



Internal ID18596285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26251764..26265278hg38UCSC Ensembl
Innerchr18:23831728..23845242hg19UCSC Ensembl
Innerchr18:22085726..22099240hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3813515
hg1913515
hg1813515
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2120253, nssv2120257, nssv2120254, nssv2120249, nssv2120255, nssv2120248, nssv2120251, nssv2120256, nssv2120252, nssv2120250
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTAF4B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961038
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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