A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17496970



Internal ID22554904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160655437..160667346hg38UCSC Ensembl
chr5:160082444..160094353hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811910
hg1911910
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841515
Supporting Variants
Samples
Known GenesATP10B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17496970
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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