A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598900



Internal ID6985948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182092953..182122975hg38UCSC Ensembl
Innerchr3:182092968..182122961hg38UCSC Ensembl
Outerchr3:182092939..182122990hg38UCSC Ensembl
chr3:181810741..181840763hg19UCSC Ensembl
Innerchr3:181810756..181840749hg19UCSC Ensembl
Outerchr3:181810727..181840778hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3830023
hg1930023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11251225
SamplesHG00284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598900
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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