A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585463



Internal ID6625781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22123042..22125013hg38UCSC Ensembl
Innerchr1:22123060..22124996hg38UCSC Ensembl
Outerchr1:22123025..22125031hg38UCSC Ensembl
chr1:22449535..22451506hg19UCSC Ensembl
Innerchr1:22449553..22451489hg19UCSC Ensembl
Outerchr1:22449518..22451524hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381972
hg191972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9889257
SamplesHG00452
Known GenesWNT4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585463
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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