A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11357363



Internal ID1359179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12121381..12230275hg38UCSC Ensembl
chr4:12123005..12231899hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38108895
hg19108895
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599671
Supporting Variants
SamplesHG01781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11357363
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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