A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977149



Internal ID20544189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100597653..100603959hg38UCSC Ensembl
chr10:102357410..102363716hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg386307
hg196307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977149
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