A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15986097



Internal ID5987913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6377364..6387673hg38UCSC Ensembl
chr19:6377375..6387684hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810310
hg1910310
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643555
Supporting Variants
SamplesHG00629
Known GenesGTF2F1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15986097
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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