A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603311



Internal ID6990343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177604618..177926179hg38UCSC Ensembl
Innerchr4:177604623..177926174hg38UCSC Ensembl
Outerchr4:177604613..177926184hg38UCSC Ensembl
chr4:178525772..178847333hg19UCSC Ensembl
Innerchr4:178525777..178847328hg19UCSC Ensembl
Outerchr4:178525767..178847338hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38321562
hg19321562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11719114
SamplesHG02769
Known GenesLINC01098, LINC01099
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603311
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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