A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540505



Internal ID20913798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42370338..42490894hg38UCSC Ensembl
chr22:42766344..42886900hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38120557
hg19120557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074567
Samples
Known GenesNFAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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