A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979855



Internal ID18615056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93877814..93885882hg38UCSC Ensembl
Innerchr3:93596658..93604726hg19UCSC Ensembl
Innerchr3:95079348..95087416hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg388069
hg198069
hg188069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2289995, nssv2289999, nssv2289996, nssv2290000, nssv2290001, nssv2289994, nssv2289993, nssv2289998, nssv2290002, nssv2289997
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPROS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979855
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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