A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3385758



Internal ID15232728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155205709..155208407hg38UCSC Ensembl
Innerchr7:155206709..155207407hg38UCSC Ensembl
Outerchr7:155204709..155209407hg38UCSC Ensembl
chr7:154997419..155000117hg19UCSC Ensembl
Innerchr7:154998419..154999117hg19UCSC Ensembl
Outerchr7:154996419..155001117hg19UCSC Ensembl
chr7:154628352..154631050hg18UCSC Ensembl
Innerchr7:154629352..154630050hg18UCSC Ensembl
Outerchr7:154627352..154632050hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695658
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3385758
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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