A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596519



Internal ID6636790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70995244..70998670hg38UCSC Ensembl
Innerchr3:70995244..70998670hg38UCSC Ensembl
Outerchr3:70995138..70998777hg38UCSC Ensembl
chr3:71044395..71047821hg19UCSC Ensembl
Innerchr3:71044395..71047821hg19UCSC Ensembl
Outerchr3:71044289..71047928hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383427
hg193427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11038247
SamplesHG02623
Known GenesFOXP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596519
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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