A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330771



Internal ID20863929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:72883400..74213803hg38UCSC Ensembl
chr1:73349083..74679487hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381330404
hg191330405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063619
Samples
Known GenesFPGT, FPGT-TNNI3K, LRRIQ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330771
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