A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1844835



Internal ID17398662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46397324..46414489hg38UCSC Ensembl
Innerchr10:47135259..47152438hg19UCSC Ensembl
Innerchr10:46555265..46572444hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817166
hg1917180
hg1817180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947931
Supporting Variants
SamplesHGDP00521
Known GenesLINC00842
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1844835
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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