A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604608



Internal ID6991636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32357219..32363950hg38UCSC Ensembl
Innerchr5:32357233..32363937hg38UCSC Ensembl
Outerchr5:32357206..32363964hg38UCSC Ensembl
chr5:32357325..32364056hg19UCSC Ensembl
Innerchr5:32357339..32364043hg19UCSC Ensembl
Outerchr5:32357312..32364070hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg386732
hg196732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11857050, essv11857048, essv11857047, essv11857049, essv11857051
SamplesHG04018, HG03911, NA21106, HG03990, HG02649
Known GenesZFR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604608
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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