A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5620677



Internal ID8968811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99264721..99278838hg38UCSC Ensembl
Outerchr7:99264684..99278888hg38UCSC Ensembl
Innerchr7:98862344..98876461hg19UCSC Ensembl
Outerchr7:98862307..98876511hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814205
hg1914205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661738
Supporting Variants
SamplesHG00537
Known GenesMYH16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5620677
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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