A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11541561



Internal ID1291056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97804332..98020273hg38UCSC Ensembl
Innerchr4:97804373..98020232hg38UCSC Ensembl
Outerchr4:97804291..98020314hg38UCSC Ensembl
chr4:98725483..98941424hg19UCSC Ensembl
Innerchr4:98725524..98941383hg19UCSC Ensembl
Outerchr4:98725442..98941465hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38215942
hg19215942
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601528
Supporting Variants
SamplesHG01134
Known GenesSTPG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11541561
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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