A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811761



Internal ID21257099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139398760..139399053hg38UCSC Ensembl
chr5:138734449..138734742hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702437
Samples
Known GenesSPATA24
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811761
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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