A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150035



Internal ID21423315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94773920..94774248hg38UCSC Ensembl
chr5:94109625..94109953hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583095
Supporting Variants
SamplesHG00731
Known GenesMCTP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150035
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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