A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667397



Internal ID9586816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31817616..31829810hg38UCSC Ensembl
chr6:31785393..31797587hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3812195
hg1912195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6223575, essv6389129
SamplesNA18986, NA18989
Known GenesHSPA1A, HSPA1B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667397
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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