A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945852



Internal ID18246016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27967310..27968423hg38UCSC Ensembl
Innerchr1:28293821..28294934hg19UCSC Ensembl
Innerchr1:28166408..28167521hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381114
hg191114
hg181114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1757667, nssv1757669, nssv1757660, nssv1757661, nssv1757663, nssv1757664, nssv1757665, nssv1757662, nssv1757668, nssv1757666
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesXKR8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945852
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