A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6025737



Internal ID9569955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51874326..51875074hg38UCSC Ensembl
chr5:51170160..51170908hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659035
Supporting Variants
SamplesNA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6025737
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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