A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127156



Internal ID20694196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132997079..133006905hg38UCSC Ensembl
chr5:132332771..132342597hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg389827
hg199827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407560
Supporting Variants
Samples
Known GenesZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127156
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