A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3430958



Internal ID15277914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32531416..32531416hg38UCSC Ensembl
Innerchr7:32531415..32531417hg38UCSC Ensembl
Outerchr7:32531376..32531436hg38UCSC Ensembl
chr7:32571028..32571028hg19UCSC Ensembl
Innerchr7:32571027..32571029hg19UCSC Ensembl
Outerchr7:32570988..32571048hg19UCSC Ensembl
chr7:32537553..32537553hg18UCSC Ensembl
Innerchr7:32537554..32537552hg18UCSC Ensembl
Outerchr7:32537513..32537573hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3864
hg1964
hg1864
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8648387
Samples
Known GenesAVL9
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3430958
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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