A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977985



Internal ID18613190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57320300..57340892hg38UCSC Ensembl
Innerchr16:57354212..57374804hg19UCSC Ensembl
Innerchr16:55911713..55932305hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3820593
hg1920593
hg1820593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2062514, nssv2062518, nssv2062515, nssv2062519, nssv2062521, nssv2062517, nssv2062512, nssv2062513, nssv2062520, nssv2062516
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)nsv977985
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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