A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9892762



Internal ID6518055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25266151..25334731hg38UCSC Ensembl
chr1:25592642..25661222hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3868581
hg1968581
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585521
Supporting Variants
SamplesHG03937
Known GenesRHD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9892762
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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