A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644330



Internal ID6684398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39515085..39517330hg38UCSC Ensembl
Innerchr19:39515097..39517319hg38UCSC Ensembl
Outerchr19:39515074..39517342hg38UCSC Ensembl
chr19:40005725..40007970hg19UCSC Ensembl
Innerchr19:40005737..40007959hg19UCSC Ensembl
Outerchr19:40005714..40007982hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16054563, essv16054561, essv16054564, essv16054562, essv16054560
SamplesHG02187, HG02164, HG01797, HG01857, HG01845
Known GenesSELV
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644330
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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