A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981441



Internal ID18616638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25065681..25068031hg38UCSC Ensembl
Innerchr7:25105300..25107650hg19UCSC Ensembl
Innerchr7:25071825..25074175hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382351
hg192351
hg182351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2440035, nssv2440041, nssv2440036, nssv2440040, nssv2440037, nssv2440038, nssv2440033, nssv2440034, nssv2440042, nssv2440039
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981441
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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