A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767355



Internal ID19306464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36597956..36598357hg38UCSC Ensembl
chr2:36825099..36825500hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071587
Supporting Variants
SamplesKWP1
Known GenesFEZ2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767355
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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