A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763354



Internal ID19308749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125158830..125161231hg38UCSC Ensembl
chr10:126847399..126849800hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069088
Supporting Variants
SamplesKWP1
Known GenesCTBP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763354
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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