A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604439



Internal ID6991467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26009361..26011645hg38UCSC Ensembl
Innerchr5:26009362..26011644hg38UCSC Ensembl
Outerchr5:26009360..26011646hg38UCSC Ensembl
chr5:26009470..26011754hg19UCSC Ensembl
Innerchr5:26009471..26011753hg19UCSC Ensembl
Outerchr5:26009469..26011755hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11845547, essv11845541, essv11845546, essv11845545, essv11845550, essv11845544, essv11845543, essv11845548, essv11845542, essv11845549
SamplesHG03280, NA19393, HG03436, NA19138, NA19024, HG03054, NA18933, NA19436, NA19037, NA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604439
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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