A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672772



Internal ID9592191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134538191..134576960hg38UCSC Ensembl
chr7:134222943..134261712hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3838770
hg1938770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1240e199
Supporting Variantsessv6069791
SamplesNA18528
Known GenesAKR1B10, AKR1B15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672772
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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