A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564916



Internal ID18765992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163580814..163581072hg38UCSC Ensembl
Outerchr4:163580769..163581132hg38UCSC Ensembl
Innerchr4:164501966..164502224hg19UCSC Ensembl
Outerchr4:164501921..164502284hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763663
Samples
Known GenesMARCH1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564916
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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