A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601528



Internal ID6988565
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11541562, essv11541563, essv11541564, essv11541561
SamplesHG01134, HG01435, HG01142, HG01260
Known GenesSTPG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601528
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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