A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601186



Internal ID6988225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82971204..82975207hg38UCSC Ensembl
Innerchr4:82971204..82975207hg38UCSC Ensembl
Outerchr4:82971052..82975350hg38UCSC Ensembl
chr4:83892357..83896360hg19UCSC Ensembl
Innerchr4:83892357..83896360hg19UCSC Ensembl
Outerchr4:83892205..83896503hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg384004
hg194004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11521116, essv11521117
SamplesHG01177, HG01182
Known GenesLIN54
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601186
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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