A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977711



Internal ID18612917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45070454..45081201hg38UCSC Ensembl
Innerchr15:45362652..45373399hg19UCSC Ensembl
Innerchr15:43149944..43160691hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3810748
hg1910748
hg1810748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2022472, nssv2022469, nssv2022473, nssv2022474, nssv2022476, nssv2022477, nssv2022475, nssv2022470, nssv2022468, nssv2022471
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSORD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977711
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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