A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968608



Internal ID18603836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33785534..33814266hg38UCSC Ensembl
Innerchr9:33785532..33814264hg19UCSC Ensembl
Innerchr9:33775532..33804264hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3828733
hg1928733
hg1828733
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2528121, nssv2528120, nssv2528122, nssv2528114, nssv2528115, nssv2528117, nssv2528113, nssv2528116, nssv2528118, nssv2528119
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPRSS3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968608
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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