A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970469



Internal ID18605691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39866778..39873693hg38UCSC Ensembl
Innerchr7:39906377..39913292hg19UCSC Ensembl
Innerchr7:39872902..39879817hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386916
hg196916
hg186916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2445866, nssv2445860, nssv2445865, nssv2445863, nssv2445867, nssv2445869, nssv2445862, nssv2445861, nssv2445868, nssv2445864
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)nsv970469
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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