A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575002



Internal ID21767045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117373257..117373257hg38UCSC Ensembl
chr7:117013311..117013311hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072304
Supporting Variants
Samples
Known GenesASZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575002
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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