A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605850



Internal ID6992787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96117495..96180719hg38UCSC Ensembl
Innerchr5:96117531..96180683hg38UCSC Ensembl
Outerchr5:96117459..96180755hg38UCSC Ensembl
chr5:95453199..95516423hg19UCSC Ensembl
Innerchr5:95453235..95516387hg19UCSC Ensembl
Outerchr5:95453163..95516459hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3863225
hg1963225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11983363
SamplesHG01104
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605850
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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