A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1857558



Internal ID17498526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74525280..74530420hg38UCSC Ensembl
Innerchr10:76285038..76290178hg19UCSC Ensembl
Innerchr10:75955044..75960184hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg385141
hg195141
hg185141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948072
Supporting Variants
SamplesHGDP01029
Known GenesADK
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)nssv1857558
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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