A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975796



Internal ID18611003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35028681..35032938hg38UCSC Ensembl
Innerchr10:35317609..35321866hg19UCSC Ensembl
Innerchr10:35357615..35361872hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384258
hg194258
hg184258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758642
SamplesHGDP00998
Known GenesCUL2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975796
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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