A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766577



Internal ID18968063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176817298..176818199hg38UCSC Ensembl
chr5:176244299..176245200hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074890
Supporting Variants
SamplesKWP1
Known GenesUNC5A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766577
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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