A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107464



Internal ID2999341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58257210..58265558hg38UCSC Ensembl
chr19:58768576..58776924hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg388349
hg198349
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644930
Supporting Variants
SamplesHG02646
Known GenesZNF544
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107464
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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