A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614455



Internal ID6654661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107173526..107176671hg38UCSC Ensembl
Innerchr7:107173554..107176643hg38UCSC Ensembl
Outerchr7:107173498..107176699hg38UCSC Ensembl
chr7:106813971..106817116hg19UCSC Ensembl
Innerchr7:106813999..106817088hg19UCSC Ensembl
Outerchr7:106813943..106817144hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383146
hg193146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12917696
SamplesHG03652
Known GenesHBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614455
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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