A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607097



Internal ID6994032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147798673..147807764hg38UCSC Ensembl
Innerchr5:147798673..147807764hg38UCSC Ensembl
Outerchr5:147798303..147807949hg38UCSC Ensembl
chr5:147178236..147187327hg19UCSC Ensembl
Innerchr5:147178236..147187327hg19UCSC Ensembl
Outerchr5:147177866..147187512hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg389092
hg199092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12092489, essv12092490, essv12092493, essv12092491, essv12092492
SamplesHG03479, HG02976, NA19321, HG03461, HG02646
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607097
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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