A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6043773



Internal ID9710637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2712601..2715236hg38UCSC Ensembl
chr5:2712715..2715350hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382636
hg192636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657538
Supporting Variants
SamplesNA19462
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6043773
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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