A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602805



Internal ID6643061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157127728..157128678hg38UCSC Ensembl
Innerchr4:157127753..157128654hg38UCSC Ensembl
Outerchr4:157127704..157128703hg38UCSC Ensembl
chr4:158048880..158049830hg19UCSC Ensembl
Innerchr4:158048905..158049806hg19UCSC Ensembl
Outerchr4:158048856..158049855hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38951
hg19951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11659911
SamplesHG02152
Known GenesGLRB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602805
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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