A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598703



Internal ID6985838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173734521..173735664hg38UCSC Ensembl
Innerchr3:173734535..173735651hg38UCSC Ensembl
Outerchr3:173734508..173735678hg38UCSC Ensembl
chr3:173452311..173453454hg19UCSC Ensembl
Innerchr3:173452325..173453441hg19UCSC Ensembl
Outerchr3:173452298..173453468hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381144
hg191144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11228981
SamplesHG03112
Known GenesNLGN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598703
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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