A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074181



Internal ID18979793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13013999..13019100hg38UCSC Ensembl
chr10:13055999..13061100hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771016
SamplesKWP1
Known GenesCCDC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074181
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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