A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602431



Internal ID6989465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139045595..139046662hg38UCSC Ensembl
Innerchr4:139045648..139046609hg38UCSC Ensembl
Outerchr4:139045542..139046715hg38UCSC Ensembl
chr4:139966749..139967816hg19UCSC Ensembl
Innerchr4:139966802..139967763hg19UCSC Ensembl
Outerchr4:139966696..139967869hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11632897
SamplesHG03917
Known GenesCCRN4L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602431
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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