A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1836817



Internal ID17811002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31364251..31365952hg38UCSC Ensembl
Innerchr10:31653180..31654881hg19UCSC Ensembl
Innerchr10:31693186..31694887hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381702
hg191702
hg181702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947817
Supporting Variants
SamplesHGDP00927
Known GenesZEB1
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)nssv1836817
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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