A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740945



Internal ID18715191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103625882..103627504hg38UCSC Ensembl
Outerchr7:103625663..103627684hg38UCSC Ensembl
Innerchr7:103266329..103267951hg19UCSC Ensembl
Outerchr7:103266110..103268131hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542198
Supporting Variants
Samples
Known GenesRELN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740945
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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