A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740984



Internal ID18715230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106628424..106629181hg38UCSC Ensembl
Outerchr7:106628386..106629294hg38UCSC Ensembl
Innerchr7:106268870..106269627hg19UCSC Ensembl
Outerchr7:106268832..106269740hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740984
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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