A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811805



Internal ID21257143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60819086..60819135hg38UCSC Ensembl
chr5:60114913..60114962hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705590
Samples
Known GenesELOVL7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811805
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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