A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1839736



Internal ID17877336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36522258..36522966hg38UCSC Ensembl
Innerchr10:36811186..36811894hg19UCSC Ensembl
Innerchr10:36851192..36851900hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947838
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)nssv1839736
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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