A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644693



Internal ID7031447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52390478..52468038hg38UCSC Ensembl
chr19:52893731..52971291hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3877561
hg1977561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16083570
SamplesHG01954
Known GenesZNF528, ZNF534, ZNF578
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644693
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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