A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663277



Internal ID9929382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149997453..149998045hg38UCSC Ensembl
chr5:149377016..149377608hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6579232, essv6439751, essv6523982, essv6395100, essv6463852, essv6387180
SamplesNA19704, HG00736, NA19236, NA19625, NA19428, NA19223
Known GenesTIGD6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663277
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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