A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410352



Internal ID21067905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81616091..81616831hg38UCSC Ensembl
chr5:80911910..80912650hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132912
Samples
Known GenesSSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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