A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587653



Internal ID6627954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157587056..157588902hg38UCSC Ensembl
Innerchr1:157587056..157588902hg38UCSC Ensembl
Outerchr1:157586831..157589120hg38UCSC Ensembl
chr1:157556846..157558692hg19UCSC Ensembl
Innerchr1:157556846..157558692hg19UCSC Ensembl
Outerchr1:157556621..157558910hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381847
hg191847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10156764
SamplesNA19472
Known GenesFCRL4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587653
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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