A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607351



Internal ID6994285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159894760..159897261hg38UCSC Ensembl
Innerchr5:159894783..159897239hg38UCSC Ensembl
Outerchr5:159894738..159897284hg38UCSC Ensembl
chr5:159321767..159324268hg19UCSC Ensembl
Innerchr5:159321790..159324246hg19UCSC Ensembl
Outerchr5:159321745..159324291hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12115656
SamplesHG02477
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607351
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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