A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6395646



Internal ID9373049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137888261..137889083hg38UCSC Ensembl
chr7:137573007..137573829hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675854
Supporting Variants
SamplesNA12004
Known GenesCREB3L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6395646
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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