A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763663



Internal ID18737909
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 StatusS
Merged Variantsesv3564916
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763663
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer