A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605703



Internal ID6992641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86256488..86260260hg38UCSC Ensembl
Innerchr5:86256511..86260238hg38UCSC Ensembl
Outerchr5:86256466..86260283hg38UCSC Ensembl
chr5:85552306..85556078hg19UCSC Ensembl
Innerchr5:85552329..85556056hg19UCSC Ensembl
Outerchr5:85552284..85556101hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383773
hg193773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11965043
SamplesHG03367
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605703
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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