A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6340156



Internal ID9699032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153747243..153752405hg38UCSC Ensembl
chr3:153465032..153470194hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg385163
hg195163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659707
Supporting Variants
SamplesNA19449
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6340156
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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