A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16089185



Internal ID2779676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53096367..53124914hg38UCSC Ensembl
chr19:53599620..53628167hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3828548
hg1928548
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644737
Supporting Variants
SamplesHG02450
Known GenesZNF160, ZNF415
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16089185
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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