A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3391755



Internal ID15238721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155334252..155335173hg38UCSC Ensembl
Innerchr7:155334252..155335173hg38UCSC Ensembl
Outerchr7:155333797..155336360hg38UCSC Ensembl
chr7:155125962..155126883hg19UCSC Ensembl
Innerchr7:155125962..155126883hg19UCSC Ensembl
Outerchr7:155125507..155128599hg19UCSC Ensembl
chr7:154819708..154820629hg18UCSC Ensembl
Innerchr7:154819708..154820629hg18UCSC Ensembl
Outerchr7:154819253..154821816hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38922
hg19922
hg18922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652359
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3391755
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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