A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647735



Internal ID6687789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38509211..38512874hg38UCSC Ensembl
Innerchr22:38509213..38512872hg38UCSC Ensembl
Outerchr22:38509209..38512876hg38UCSC Ensembl
chr22:38905216..38908879hg19UCSC Ensembl
Innerchr22:38905218..38908877hg19UCSC Ensembl
Outerchr22:38905214..38908881hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383664
hg193664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16421464, essv16421460, essv16421459, essv16421463, essv16421461, essv16421462, essv16421458
SamplesHG02852, HG03082, HG03040, HG03055, HG02666, HG02896, HG03066
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647735
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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