A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974561



Internal ID18263086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40035873..40036572hg38UCSC Ensembl
Innerchr15:40328074..40328773hg19UCSC Ensembl
Innerchr15:38115366..38116065hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38700
hg19700
hg18700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2018972, nssv2018968, nssv2018971, nssv2018969, nssv2018966, nssv2018965, nssv2018967, nssv2018973, nssv2018970, nssv2018964
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSRP14
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974561
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer