A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250408



Internal ID20817448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35510714..35512288hg38UCSC Ensembl
chr1:35976315..35977889hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541604
Supporting Variants
Samples
Known GenesKIAA0319L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250408
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer