A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15977386



Internal ID1981579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3805735..3814064hg38UCSC Ensembl
chr19:3805733..3814062hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388330
hg198330
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643475
Supporting Variants
SamplesHG01843
Known GenesZFR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15977386
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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