A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762752



Internal ID18965223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134955094..134955715hg38UCSC Ensembl
chr3:134673936..134674557hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074627
Supporting Variants
SamplesKWP1
Known GenesEPHB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762752
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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