A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741282



Internal ID18715528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141791916..141792097hg38UCSC Ensembl
Outerchr7:141791864..141792127hg38UCSC Ensembl
Innerchr7:141491716..141491897hg19UCSC Ensembl
Outerchr7:141491664..141491927hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741282
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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