A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346686



Internal ID21004239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211562794..211790074hg38UCSC Ensembl
chr2:212427519..212654799hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38227281
hg19227281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083320
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346686
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