A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414735



Internal ID21072288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151514773..151515578hg38UCSC Ensembl
chr5:150894334..150895139hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128711
Samples
Known GenesFAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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