A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3396645



Internal ID15243608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155791966..155792657hg38UCSC Ensembl
Innerchr7:155791966..155792657hg38UCSC Ensembl
Outerchr7:155791513..155793078hg38UCSC Ensembl
chr7:155584660..155585351hg19UCSC Ensembl
Innerchr7:155584660..155585351hg19UCSC Ensembl
Outerchr7:155584207..155585772hg19UCSC Ensembl
chr7:155277421..155278112hg18UCSC Ensembl
Innerchr7:155277421..155278112hg18UCSC Ensembl
Outerchr7:155276968..155278533hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38692
hg19692
hg18692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652360
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3396645
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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