A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764216



Internal ID18965359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155733561..155736439hg38UCSC Ensembl
chr4:156654713..156657591hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382879
hg192879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073383
Supporting Variants
SamplesKWP1
Known GenesGUCY1A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764216
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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