A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400892



Internal ID21058445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151324431..151332010hg38UCSC Ensembl
chr5:150703992..150711571hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg387580
hg197580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213298
Samples
Known GenesSLC36A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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