A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966866



Internal ID18255409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100180714..100195131hg38UCSC Ensembl
Innerchr7:99778337..99792754hg19UCSC Ensembl
Innerchr7:99616273..99630690hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814418
hg1914418
hg1814418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2472352, nssv2472354, nssv2472356, nssv2472357, nssv2472350, nssv2472353, nssv2472351, nssv2472355, nssv2472358, nssv2472349
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSTAG3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966866
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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