A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6174049



Internal ID9816274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24057529..24075323hg38UCSC Ensembl
chr7:24097148..24114942hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817795
hg1917795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666861
Supporting Variants
SamplesNA19982
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6174049
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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