A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660794



Internal ID9926899
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5423518, essv6288524, essv5984803, essv5565184, essv5904019
SamplesNA19701, NA19920, NA18868, NA19235, NA19982
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660794
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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