A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1867314



Internal ID17737674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106549236..106551523hg38UCSC Ensembl
Innerchr10:108308994..108311281hg19UCSC Ensembl
Innerchr10:108298984..108301271hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382288
hg192288
hg182288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948179
Supporting Variants
SamplesHGDP00456
Known Genes
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)nssv1867314
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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