A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6391858



Internal ID9369261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180639155..180639304hg38UCSC Ensembl
chr5:180066155..180066304hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665740
Supporting Variants
SamplesHG00536
Known GenesFLT4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6391858
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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