A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644544



Internal ID6684611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47070055..47070982hg38UCSC Ensembl
Innerchr19:47070058..47070980hg38UCSC Ensembl
Outerchr19:47070053..47070985hg38UCSC Ensembl
chr19:47573312..47574239hg19UCSC Ensembl
Innerchr19:47573315..47574237hg19UCSC Ensembl
Outerchr19:47573310..47574242hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16070986, essv16070983, essv16070985, essv16070987, essv16070984, essv16070988, essv16070982
SamplesHG02810, HG03046, NA20362, HG03485, NA19102, HG02804, HG03045
Known GenesZC3H4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644544
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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