A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16041343



Internal ID6043159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33097929..33098510hg38UCSC Ensembl
Innerchr19:33097945..33098494hg38UCSC Ensembl
Outerchr19:33097913..33098526hg38UCSC Ensembl
chr19:33588835..33589416hg19UCSC Ensembl
Innerchr19:33588851..33589400hg19UCSC Ensembl
Outerchr19:33588819..33589432hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644181
Supporting Variants
SamplesHG03157
Known GenesGPATCH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16041343
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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