A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600998



Internal ID6988037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73609863..73613883hg38UCSC Ensembl
Innerchr4:73609867..73613879hg38UCSC Ensembl
Outerchr4:73609859..73613887hg38UCSC Ensembl
chr4:74475580..74479600hg19UCSC Ensembl
Innerchr4:74475584..74479596hg19UCSC Ensembl
Outerchr4:74475576..74479604hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg384021
hg194021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11501501, essv11501502
SamplesNA19082, NA19080
Known GenesRASSF6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600998
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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