A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1858244



Internal ID17465356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74370569..74372427hg38UCSC Ensembl
Innerchr10:76130327..76132185hg19UCSC Ensembl
Innerchr10:75800333..75802191hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381859
hg191859
hg181859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948071
Supporting Variants
SamplesHGDP00927
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)nssv1858244
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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