A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601136



Internal ID6988175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80377603..80385091hg38UCSC Ensembl
Innerchr4:80378103..80384591hg38UCSC Ensembl
Outerchr4:80376603..80386091hg38UCSC Ensembl
chr4:81298757..81306245hg19UCSC Ensembl
Innerchr4:81299257..81305745hg19UCSC Ensembl
Outerchr4:81297757..81307245hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg387489
hg197489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11516780
SamplesHG01070
Known GenesC4orf22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601136
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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