A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948179



Internal ID18595025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106549236..106551523hg38UCSC Ensembl
Innerchr10:108308994..108311281hg19UCSC Ensembl
Innerchr10:108298984..108301271hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382288
hg192288
hg182288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1867317, nssv1867314, nssv1867312, nssv1867311, nssv1867315, nssv1867313, nssv1867318, nssv1867309, nssv1867316, nssv1867310
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)nsv948179
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