A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644303



Internal ID6684371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38056836..38058799hg38UCSC Ensembl
Innerchr19:38056842..38058794hg38UCSC Ensembl
Outerchr19:38056831..38058805hg38UCSC Ensembl
chr19:38547476..38549439hg19UCSC Ensembl
Innerchr19:38547482..38549434hg19UCSC Ensembl
Outerchr19:38547471..38549445hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg381964
hg191964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16052164
SamplesHG02570
Known GenesSIPA1L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644303
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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