A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772747



Internal ID19306208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166570347..166571148hg38UCSC Ensembl
chr4:167491499..167492300hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073813
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772747
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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