A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765076



Internal ID19315175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117542688..117543689hg38UCSC Ensembl
chr10:119302199..119303200hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069966
Supporting Variants
SamplesKWP1
Known GenesEMX2, EMX2OS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765076
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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