A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5811288



Internal ID9717838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71877223..71877865hg38UCSC Ensembl
chr5:71173050..71173692hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670819
Supporting Variants
SamplesNA19469
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5811288
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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