A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11360276



Internal ID3290699
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599747
Supporting Variants
SamplesHG02923
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11360276
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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