A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597104



Internal ID6984418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97837412..97842145hg38UCSC Ensembl
Innerchr3:97837412..97842145hg38UCSC Ensembl
Outerchr3:97837286..97842323hg38UCSC Ensembl
chr3:97556256..97560989hg19UCSC Ensembl
Innerchr3:97556256..97560989hg19UCSC Ensembl
Outerchr3:97556130..97561167hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11074786
SamplesHG02017
Known GenesCRYBG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597104
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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