A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596524



Internal ID6983839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71376285..71379557hg38UCSC Ensembl
Innerchr3:71376307..71379535hg38UCSC Ensembl
Outerchr3:71376263..71379579hg38UCSC Ensembl
chr3:71425436..71428708hg19UCSC Ensembl
Innerchr3:71425458..71428686hg19UCSC Ensembl
Outerchr3:71425414..71428730hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383273
hg193273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11038356
SamplesNA20804
Known GenesFOXP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596524
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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