A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771766



Internal ID18957957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110497941..110498442hg38UCSC Ensembl
chr10:112257699..112258200hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069964
Supporting Variants
SamplesKWP1
Known GenesDUSP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771766
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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