A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350065



Internal ID21007618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10383134..10384839hg38UCSC Ensembl
chr2:10523260..10524965hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381706
hg191706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075070
Samples
Known GenesHPCAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350065
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