A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379657



Internal ID21037210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9895384..9897470hg38UCSC Ensembl
chr5:9895496..9897582hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382087
hg192087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136257
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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