A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323815



Internal ID20856937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70982841..70983457hg38UCSC Ensembl
chr1:71448524..71449140hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062841
Samples
Known GenesPTGER3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323815
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