A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077318



Internal ID18978467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27927270..27929371hg38UCSC Ensembl
chr10:28216199..28218300hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766307
SamplesKWP1
Known GenesARMC4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077318
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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