A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970783



Internal ID18606005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20878..38678hg38UCSC Ensembl
Innerchr7:20878..38678hg19UCSC Ensembl
Innerchr7:116401..133761hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3817801
hg1917801
hg1817361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2432918, nssv2432924, nssv2432921, nssv2432916, nssv2432922, nssv2432915, nssv2432917, nssv2432923, nssv2432920, nssv2432919
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)nsv970783
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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