A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378853



Internal ID21036406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21578271..21578884hg38UCSC Ensembl
chr5:21578380..21578993hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128185
Samples
Known GenesGUSBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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