A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602976



Internal ID6990009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163921938..163935251hg38UCSC Ensembl
Innerchr4:163921970..163935219hg38UCSC Ensembl
Outerchr4:163921906..163935283hg38UCSC Ensembl
chr4:164843090..164856403hg19UCSC Ensembl
Innerchr4:164843122..164856371hg19UCSC Ensembl
Outerchr4:164843058..164856435hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3813314
hg1913314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11676111
SamplesHG01938
Known GenesMARCH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602976
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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