A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948111



Internal ID18594957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86985611..87028511hg38UCSC Ensembl
Innerchr10:88745368..88788268hg19UCSC Ensembl
Innerchr10:88735348..88778248hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3842901
hg1942901
hg1842901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1861106, nssv1861102, nssv1861109, nssv1861107, nssv1861103, nssv1861105, nssv1861104, nssv1861111, nssv1861110, nssv1861108
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP11, FAM25A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948111
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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