A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8695659



Internal ID15054332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155614997..155617695hg38UCSC Ensembl
Innerchr7:155615997..155616695hg38UCSC Ensembl
Outerchr7:155613997..155618695hg38UCSC Ensembl
chr7:155407691..155410389hg19UCSC Ensembl
Innerchr7:155408691..155409389hg19UCSC Ensembl
Outerchr7:155406691..155411389hg19UCSC Ensembl
chr7:155100452..155103150hg18UCSC Ensembl
Innerchr7:155101452..155102150hg18UCSC Ensembl
Outerchr7:155099452..155104150hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3401073
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8695659
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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