A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981506



Internal ID18616703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66377707..66411886hg38UCSC Ensembl
Innerchr7:65842694..65876873hg19UCSC Ensembl
Innerchr7:65480129..65514308hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3834180
hg1934180
hg1834180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2458598, nssv2458593, nssv2458595, nssv2458591, nssv2458600, nssv2458592, nssv2458594, nssv2458597, nssv2458599, nssv2458596
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00174
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981506
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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