A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538774



Internal ID20912088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29445909..29773499hg38UCSC Ensembl
chr22:29841898..30169488hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38327591
hg19327591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204975
Samples
Known GenesCABP7, NEFH, NF2, NIPSNAP1, THOC5, UQCR10, ZMAT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer