A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5884729



Internal ID9657807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156531938..156542821hg38UCSC Ensembl
chr7:156324632..156335515hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3810884
hg1910884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658442
Supporting Variants
SamplesNA19390
Known GenesLINC00244, LINC01006
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5884729
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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