A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349347



Internal ID21006900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167167517..167221440hg38UCSC Ensembl
chr2:168024027..168077950hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3853924
hg1953924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080289
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349347
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