A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11989781



Internal ID1736305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98480160..98575434hg38UCSC Ensembl
chr5:97815864..97911138hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3895275
hg1995275
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3605915
Supporting Variants
SamplesHG01607
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11989781
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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