A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565964



Internal ID21758007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130042123..130045816hg38UCSC Ensembl
chr7:129681963..129685656hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg383694
hg193694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000839
Supporting Variants
Samples
Known GenesZC3HC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565964
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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