A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1861104



Internal ID17795679
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 StatusS
Merged Variantsnsv948111
Supporting Variants
SamplesHGDP00778
Known GenesAGAP11, FAM25A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1861104
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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