A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453651



Internal ID22511525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44931110..44933651hg38UCSC Ensembl
chr10:45426558..45429099hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382542
hg192542
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865321
Supporting Variants
Samples
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453651
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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