A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544960



Internal ID20918198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38350494..38358690hg38UCSC Ensembl
chr22:38746499..38754695hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg388197
hg198197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073961
Samples
Known GenesLOC400927
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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