A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979838



Internal ID18615039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61742120..61743432hg38UCSC Ensembl
Innerchr3:61727794..61729106hg19UCSC Ensembl
Innerchr3:61702834..61704146hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381313
hg191313
hg181313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2282015, nssv2282016, nssv2282012, nssv2282019, nssv2282018, nssv2282014, nssv2282017, nssv2282011, nssv2282020, nssv2282013
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPTPRG
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979838
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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