A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607540



Internal ID6647780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168903334..168904074hg38UCSC Ensembl
Innerchr5:168903373..168904036hg38UCSC Ensembl
Outerchr5:168903296..168904113hg38UCSC Ensembl
chr5:168330339..168331079hg19UCSC Ensembl
Innerchr5:168330378..168331041hg19UCSC Ensembl
Outerchr5:168330301..168331118hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12126988
SamplesHG02012
Known GenesSLIT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607540
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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