A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976897



Internal ID18612103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25082558..25083747hg38UCSC Ensembl
Innerchr15:25327705..25328894hg19UCSC Ensembl
Innerchr15:22878798..22879987hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381190
hg191190
hg181190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2011678, nssv2011674, nssv2011669, nssv2011677, nssv2011673, nssv2011670, nssv2011676, nssv2011671, nssv2011675, nssv2011672
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSNORD116-16, SNORD116-17, SNORD116-19
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976897
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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