A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659247



Internal ID3908688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155471016..155478171hg38UCSC Ensembl
Innerchr4:155471516..155477671hg38UCSC Ensembl
Outerchr4:155470016..155479171hg38UCSC Ensembl
chr4:156392168..156399323hg19UCSC Ensembl
Innerchr4:156392668..156398823hg19UCSC Ensembl
Outerchr4:156391168..156400323hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387156
hg197156
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602760
Supporting Variants
SamplesHG03563
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659247
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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