A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811291



Internal ID21256629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180617727..180618230hg38UCSC Ensembl
chr5:180044727..180045230hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699502
Samples
Known GenesFLT4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811291
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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