A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323184



Internal ID20856300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10308401..10318600hg38UCSC Ensembl
chr1:10368459..10378658hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv45n223
Supporting Variantsnssv18050162
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323184
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