A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509567



Internal ID22567517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117369763..117370908hg38UCSC Ensembl
chr7:117009817..117010962hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865185
Supporting Variants
Samples
Known GenesASZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509567
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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