A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740256



Internal ID18714502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38473451..38473711hg38UCSC Ensembl
Outerchr7:38473375..38473776hg38UCSC Ensembl
Innerchr7:38513051..38513311hg19UCSC Ensembl
Outerchr7:38512975..38513376hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541509
Supporting Variants
Samples
Known GenesAMPH
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740256
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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