A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669756



Internal ID9589175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134525343..134560371hg38UCSC Ensembl
chr7:134210095..134245123hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3835029
hg1935029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6238669
SamplesNA20533
Known GenesAKR1B10, AKR1B15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669756
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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