A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5449372



Internal ID9734261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137149702..137150004hg38UCSC Ensembl
chr7:136834449..136834751hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658351
Supporting Variants
SamplesNA19660
Known GenesLOC349160
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5449372
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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