A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598467



Internal ID6985603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163715932..163719968hg38UCSC Ensembl
Innerchr3:163715938..163719962hg38UCSC Ensembl
Outerchr3:163715926..163719974hg38UCSC Ensembl
chr3:163433720..163437756hg19UCSC Ensembl
Innerchr3:163433726..163437750hg19UCSC Ensembl
Outerchr3:163433714..163437762hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg384037
hg194037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11213115, essv11213116, essv11213117
SamplesNA21097, NA20864, NA20901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598467
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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