A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335909



Internal ID20993462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167048180..167048803hg38UCSC Ensembl
chr2:167904690..167905313hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080274
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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