A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976930



Internal ID18612136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44962093..44971078hg38UCSC Ensembl
Innerchr15:45254291..45263276hg19UCSC Ensembl
Innerchr15:43041583..43050568hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388986
hg198986
hg188986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2021391, nssv2021386, nssv2021387, nssv2021392, nssv2021388, nssv2021389, nssv2021393, nssv2021390, nssv2021385, nssv2021394
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC15orf43
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976930
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