A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502757



Internal ID22560698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73464851..73466750hg38UCSC Ensembl
chr7:72879181..72881080hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853530
Supporting Variants
Samples
Known GenesBAZ1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502757
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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