A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5565184



Internal ID9750946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125607024..125609085hg38UCSC Ensembl
Outerchr6:125606987..125609135hg38UCSC Ensembl
Innerchr6:125928170..125930231hg19UCSC Ensembl
Outerchr6:125928133..125930281hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382149
hg192149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660794
Supporting Variants
SamplesNA19701
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5565184
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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