A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542490



Internal ID18743566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137149722..137149981hg38UCSC Ensembl
Outerchr7:137149668..137150044hg38UCSC Ensembl
Innerchr7:136834469..136834728hg19UCSC Ensembl
Outerchr7:136834415..136834791hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741237
Samples
Known GenesLOC349160
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542490
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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