A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597485



Internal ID6637755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116120030..116366874hg38UCSC Ensembl
chr3:115838877..116085721hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38246845
hg19246845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv922e214
Supporting Variantsessv11111207
SamplesHG01953
Known GenesLSAMP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597485
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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