A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977724



Internal ID18612930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60052756..60053988hg38UCSC Ensembl
Innerchr15:60344955..60346187hg19UCSC Ensembl
Innerchr15:58132247..58133479hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381233
hg191233
hg181233
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028419, nssv2028422, nssv2028418, nssv2028424, nssv2028420, nssv2028425, nssv2028427, nssv2028423, nssv2028421, nssv2028426
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)nsv977724
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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