A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6007341



Internal ID9111326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196334794..196335146hg38UCSC Ensembl
chr3:196061665..196062017hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677485
Supporting Variants
SamplesHG01108
Known GenesTM4SF19, TM4SF19-TCTEX1D2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6007341
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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