A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647658



Internal ID7034398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34948496..34950178hg38UCSC Ensembl
Innerchr22:34948548..34950126hg38UCSC Ensembl
Outerchr22:34948444..34950230hg38UCSC Ensembl
chr22:35344485..35346167hg19UCSC Ensembl
Innerchr22:35344537..35346115hg19UCSC Ensembl
Outerchr22:35344433..35346219hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381683
hg191683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16411335
SamplesHG02724
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647658
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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