A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977899



Internal ID18266418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10108889..10114322hg38UCSC Ensembl
Innerchr16:10202746..10208179hg19UCSC Ensembl
Innerchr16:10110247..10115680hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg385434
hg195434
hg185434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2041948, nssv2041945, nssv2041950, nssv2041944, nssv2041943, nssv2041947, nssv2041949, nssv2041942, nssv2041941, nssv2041946
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesGRIN2A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977899
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