A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595629



Internal ID6982947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26182105..26323257hg38UCSC Ensembl
Innerchr3:26182105..26323257hg38UCSC Ensembl
Outerchr3:26181605..26323757hg38UCSC Ensembl
chr3:26223596..26364748hg19UCSC Ensembl
Innerchr3:26223596..26364748hg19UCSC Ensembl
Outerchr3:26223096..26365248hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38141153
hg19141153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10954287
SamplesHG01515
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595629
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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