A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601033



Internal ID6641291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75640087..75644148hg38UCSC Ensembl
Innerchr4:75640087..75644148hg38UCSC Ensembl
Outerchr4:75639860..75644313hg38UCSC Ensembl
chr4:76565271..76569332hg19UCSC Ensembl
Innerchr4:76565271..76569332hg19UCSC Ensembl
Outerchr4:76565044..76569497hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg384062
hg194062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11505838, essv11505839
SamplesHG00182, HG00421
Known GenesG3BP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601033
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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