A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740082



Internal ID18714328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23490179..23490867hg38UCSC Ensembl
Outerchr7:23490176..23490877hg38UCSC Ensembl
Innerchr7:23529798..23530486hg19UCSC Ensembl
Outerchr7:23529795..23530496hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541335
Supporting Variants
Samples
Known GenesRPS2P32
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740082
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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