A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598694



Internal ID6985829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173507638..173601328hg38UCSC Ensembl
chr3:173225428..173319118hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3893691
hg1993691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11228747, essv11228748, essv11228746
SamplesNA18988, HG01513, NA19064
Known GenesNLGN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598694
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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