A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603922



Internal ID6990953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6955717..6966021hg38UCSC Ensembl
Innerchr5:6955717..6966021hg38UCSC Ensembl
Outerchr5:6955217..6966521hg38UCSC Ensembl
chr5:6955830..6966134hg19UCSC Ensembl
Innerchr5:6955830..6966134hg19UCSC Ensembl
Outerchr5:6955330..6966634hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3810305
hg1910305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11802107, essv11802114, essv11802111, essv11802110, essv11802109, essv11802113, essv11802115, essv11802117, essv11802112, essv11802108, essv11802116
SamplesHG03773, HG04018, HG02491, HG03793, HG04238, HG03786, HG03742, HG03871, HG04017, HG03898, HG03012
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603922
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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