A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631405



Internal ID6671532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19830520..19834052hg38UCSC Ensembl
Innerchr13:19830570..19834002hg38UCSC Ensembl
Outerchr13:19830470..19834102hg38UCSC Ensembl
chr13:20404660..20408192hg19UCSC Ensembl
Innerchr13:20404710..20408142hg19UCSC Ensembl
Outerchr13:20404610..20408242hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg383533
hg193533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14657520, essv14657519
SamplesNA19429, HG03515
Known GenesZMYM5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631405
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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