A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12906291



Internal ID916705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99264597..99278752hg38UCSC Ensembl
Innerchr7:99264638..99278712hg38UCSC Ensembl
Outerchr7:99264557..99278793hg38UCSC Ensembl
chr7:98862220..98876375hg19UCSC Ensembl
Innerchr7:98862261..98876335hg19UCSC Ensembl
Outerchr7:98862180..98876416hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814156
hg1914156
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614275
Supporting Variants
SamplesHG00537
Known GenesMYH16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12906291
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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