A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7780326



Internal ID14231391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93728065..93728066hg38UCSC Ensembl
Innerchr7:93728048..93728083hg38UCSC Ensembl
Outerchr7:93728047..93728084hg38UCSC Ensembl
chr7:93357377..93357378hg19UCSC Ensembl
Innerchr7:93357360..93357395hg19UCSC Ensembl
Outerchr7:93357359..93357396hg19UCSC Ensembl
chr7:93195313..93195314hg18UCSC Ensembl
Innerchr7:93195331..93195296hg18UCSC Ensembl
Outerchr7:93195295..93195332hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3304184
Supporting Variants
SamplesNA18579
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7780326
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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