A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1867694



Internal ID17499046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112547790..112549521hg38UCSC Ensembl
Innerchr10:114307549..114309280hg19UCSC Ensembl
Innerchr10:114297539..114299270hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381732
hg191732
hg181732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948188
Supporting Variants
SamplesHGDP01029
Known GenesVTI1A
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)nssv1867694
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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