A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975205



Internal ID18263727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77917029..77960334hg38UCSC Ensembl
Innerchr11:77628075..77671380hg19UCSC Ensembl
Innerchr11:77305723..77349028hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3843306
hg1943306
hg1843306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1897438, nssv1897444, nssv1897436, nssv1897442, nssv1897440, nssv1897441, nssv1897443, nssv1897439, nssv1897437, nssv1897445
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesINTS4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975205
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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