A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982530



Internal ID18617725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65169800..65190773hg38UCSC Ensembl
Innerchr9:70063406..70084379hg19UCSC Ensembl
Innerchr9:69353226..69374199hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820974
hg1920974
hg1820974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2747651, nssv2746795, nssv2747290, nssv2754099, nssv2748709, nssv2754710, nssv2753465, nssv2755921, nssv2753313, nssv2750423
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982530
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