A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977741



Internal ID18612947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78863252..78863752hg38UCSC Ensembl
Innerchr15:79155594..79156094hg19UCSC Ensembl
Innerchr15:76942649..76943149hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2033593, nssv2033596, nssv2033591, nssv2033592, nssv2033594, nssv2033590, nssv2033588, nssv2033595, nssv2033587, nssv2033589
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)nsv977741
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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