A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762528



Internal ID18390088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42903148..42903718hg38UCSC Ensembl
Outerchr4:42903092..42903896hg38UCSC Ensembl
Innerchr4:42905165..42905735hg19UCSC Ensembl
Outerchr4:42905109..42905913hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563781
Supporting Variants
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762528
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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