A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763664



Internal ID18737910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163595095..163595238hg38UCSC Ensembl
Outerchr4:163595092..163595242hg38UCSC Ensembl
Innerchr4:164516247..164516390hg19UCSC Ensembl
Outerchr4:164516244..164516394hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564917
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763664
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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