A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667457



Internal ID9586876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95492554..95492793hg38UCSC Ensembl
chr5:94828258..94828497hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6490901, essv6431967
SamplesNA19920, NA19818
Known GenesTTC37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667457
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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