A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977731



Internal ID18266251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70858801..70861732hg38UCSC Ensembl
Innerchr15:71151140..71154071hg19UCSC Ensembl
Innerchr15:68938194..68941125hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382932
hg192932
hg182932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2030656, nssv2028290, nssv2030654, nssv2030653, nssv2030652, nssv2030651, nssv2028291, nssv2030649, nssv2030655, nssv2030650
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLRRC49
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977731
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