A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607395



Internal ID6994329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161153641..161192086hg38UCSC Ensembl
Innerchr5:161153641..161192086hg38UCSC Ensembl
Outerchr5:161153141..161192586hg38UCSC Ensembl
chr5:160580648..160619093hg19UCSC Ensembl
Innerchr5:160580648..160619093hg19UCSC Ensembl
Outerchr5:160580148..160619593hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3838446
hg1938446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12117627
SamplesNA20866
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607395
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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