A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15967929



Internal ID5969745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:712133..716174hg38UCSC Ensembl
chr19:712133..716174hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384042
hg194042
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643362
Supporting Variants
SamplesHG01051
Known GenesPALM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15967929
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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