A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6419666



Internal ID9574089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138187335..138188692hg38UCSC Ensembl
chr7:137872081..137873438hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381358
hg191358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678673
Supporting Variants
SamplesNA19137
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6419666
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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