A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968607



Internal ID18603835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33722963..33784247hg38UCSC Ensembl
Innerchr9:33722961..33784245hg19UCSC Ensembl
Innerchr9:33712961..33774245hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3861285
hg1961285
hg1861285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2527232, nssv2527231, nssv2527233, nssv2527224, nssv2527230, nssv2527227, nssv2527225, nssv2527226, nssv2527229, nssv2527228
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC101929688, PRSS3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968607
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