A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740876



Internal ID18715122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97867018..97867334hg38UCSC Ensembl
Outerchr7:97866973..97867378hg38UCSC Ensembl
Innerchr7:97496330..97496646hg19UCSC Ensembl
Outerchr7:97496285..97496690hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3542129
Supporting Variants
Samples
Known GenesASNS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740876
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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