A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6023085



Internal ID9000488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109680594..109702300hg38UCSC Ensembl
Outerchr1:109680173..109702870hg38UCSC Ensembl
Innerchr1:110223216..110244922hg19UCSC Ensembl
Outerchr1:110222795..110245492hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3822698
hg1922698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672266
Supporting Variants
SamplesHG00285
Known GenesGSTM1, GSTM2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6023085
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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