A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1844607



Internal ID17736634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44478660..44505278hg38UCSC Ensembl
Innerchr10:44974108..45000726hg19UCSC Ensembl
Innerchr10:44294114..44320732hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3826619
hg1926619
hg1826619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947901
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1844607
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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