A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434462



Internal ID22492332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64022336..64278876hg38UCSC Ensembl
chr7:63482714..63739254hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38256541
hg19256541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927170
Supporting Variants
Samples
Known GenesLINC01005, ZNF679, ZNF727, ZNF735
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434462
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01


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