A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11983056



Internal ID1984872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95706463..95713774hg38UCSC Ensembl
Innerchr5:95706963..95713274hg38UCSC Ensembl
Outerchr5:95705463..95714774hg38UCSC Ensembl
chr5:95042167..95049478hg19UCSC Ensembl
Innerchr5:95042667..95048978hg19UCSC Ensembl
Outerchr5:95041167..95050478hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg387312
hg197312
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3605836
Supporting Variants
SamplesNA19717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11983056
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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