A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1869655



Internal ID17812582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125886503..125915974hg38UCSC Ensembl
Innerchr10:127575072..127604543hg19UCSC Ensembl
Innerchr10:127565062..127594533hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3829472
hg1929472
hg1829472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv948223
Supporting Variants
SamplesHGDP00927
Known GenesFANK1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1869655
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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