A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607634



Internal ID6994566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174582438..174584943hg38UCSC Ensembl
Innerchr5:174582488..174584893hg38UCSC Ensembl
Outerchr5:174582388..174584993hg38UCSC Ensembl
chr5:174009441..174011946hg19UCSC Ensembl
Innerchr5:174009491..174011896hg19UCSC Ensembl
Outerchr5:174009391..174011996hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg382506
hg192506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12135655
SamplesNA18606
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607634
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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