A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611853



Internal ID6652068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2806746..2808158hg38UCSC Ensembl
Innerchr7:2806746..2808158hg38UCSC Ensembl
Outerchr7:2806623..2808265hg38UCSC Ensembl
chr7:2846380..2847792hg19UCSC Ensembl
Innerchr7:2846380..2847792hg19UCSC Ensembl
Outerchr7:2846257..2847899hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg381413
hg191413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12668862
SamplesHG02006
Known GenesGNA12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611853
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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