A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599747



Internal ID6986792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16151792..16152684hg38UCSC Ensembl
Innerchr4:16151795..16152682hg38UCSC Ensembl
Outerchr4:16151790..16152687hg38UCSC Ensembl
chr4:16153415..16154307hg19UCSC Ensembl
Innerchr4:16153418..16154305hg19UCSC Ensembl
Outerchr4:16153413..16154310hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11360275, essv11360285, essv11360273, essv11360270, essv11360278, essv11360280, essv11360271, essv11360284, essv11360283, essv11360277, essv11360274, essv11360282, essv11360272, essv11360281, essv11360279, essv11360276
SamplesHG03175, NA18519, HG03267, HG03132, NA19707, HG02554, HG01941, NA18907, HG03451, NA18963, HG02256, HG01956, HG02923, NA19310, HG01886, HG02643
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599747
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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