A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979181



Internal ID20546221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31386881..31394579hg38UCSC Ensembl
chr10:31675810..31683508hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg387699
hg197699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436733
Supporting Variants
Samples
Known GenesZEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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