A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6099045



Internal ID9177496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148973013..148979673hg38UCSC Ensembl
chr7:148670105..148676765hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386661
hg196661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669468
Supporting Variants
SamplesHG01389
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6099045
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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