A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970915



Internal ID18259451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101203715..101208789hg38UCSC Ensembl
Innerchr7:100846996..100852070hg19UCSC Ensembl
Innerchr7:100633716..100638790hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385075
hg195075
hg185075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2472204, nssv2472198, nssv2472202, nssv2472201, nssv2472199, nssv2472206, nssv2472207, nssv2472203, nssv2472200, nssv2472205
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPLOD3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970915
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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