A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11992444



Internal ID1697728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99488228..99497681hg38UCSC Ensembl
chr5:98823932..98833385hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg389454
hg199454
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3605941
Supporting Variants
SamplesHG01577
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11992444
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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