A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1862627



Internal ID17531876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95590762..95597378hg38UCSC Ensembl
Innerchr10:97350519..97357135hg19UCSC Ensembl
Innerchr10:97340509..97347125hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386617
hg196617
hg186617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948146
Supporting Variants
SamplesHGDP01307
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)nssv1862627
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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