A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602643



Internal ID6989676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149897563..149911160hg38UCSC Ensembl
Innerchr4:149897563..149911160hg38UCSC Ensembl
Outerchr4:149897466..149911217hg38UCSC Ensembl
chr4:150818715..150832312hg19UCSC Ensembl
Innerchr4:150818715..150832312hg19UCSC Ensembl
Outerchr4:150818618..150832369hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3813598
hg1913598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1033e214
Supporting Variantsessv11651482
SamplesNA12889
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602643
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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