A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962360



Internal ID18250918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63467308..63483269hg38UCSC Ensembl
Innerchr17:61544669..61560630hg19UCSC Ensembl
Innerchr17:58898401..58914362hg18UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3815962
hg1915962
hg1815962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2107399, nssv2107398, nssv2107397, nssv2107401, nssv2107400, nssv2107403, nssv2107405, nssv2107404, nssv2107406, nssv2107402
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesACE
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962360
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