A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975068



Internal ID18610276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124407065..124414615hg38UCSC Ensembl
Innerchr10:126095634..126103184hg19UCSC Ensembl
Innerchr10:126085624..126093174hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387551
hg197551
hg187551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764174
SamplesHGDP00778
Known GenesOAT
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975068
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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