A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739798



Internal ID18367358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2691111..2691662hg38UCSC Ensembl
Outerchr7:2691074..2691737hg38UCSC Ensembl
Innerchr7:2730745..2731296hg19UCSC Ensembl
Outerchr7:2730708..2731371hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541051
Supporting Variants
Samples
Known GenesAMZ1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739798
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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