A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597702



Internal ID6984840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127820033..127824594hg38UCSC Ensembl
Innerchr3:127820063..127824564hg38UCSC Ensembl
Outerchr3:127820003..127824624hg38UCSC Ensembl
chr3:127538876..127543437hg19UCSC Ensembl
Innerchr3:127538906..127543407hg19UCSC Ensembl
Outerchr3:127538846..127543467hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg384562
hg194562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11135436
SamplesHG02052
Known GenesMGLL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597702
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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