A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668849



Internal ID9588268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156789852..156790808hg38UCSC Ensembl
chr7:156582546..156583502hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5569768, essv5685687, essv5554263
SamplesNA19399, NA19236, NA19213
Known GenesLMBR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668849
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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