A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349948



Internal ID21007501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74060646..74061595hg38UCSC Ensembl
chr2:74287773..74288722hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090368
Samples
Known GenesTET3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349948
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