A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504841



Internal ID22562785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2762570..2769341hg38UCSC Ensembl
chr7:2802204..2808975hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg386772
hg196772
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846914
Supporting Variants
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504841
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