A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10151138



Internal ID152954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153189290..153192697hg38UCSC Ensembl
chr1:153161766..153165173hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383408
hg193408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587578
Supporting Variants
SamplesHG01894
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10151138
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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