A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583095



Internal ID21531616
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 StatusM
Merged Variants
Supporting Variantsnssv17150035
SamplesHG00731
Known GenesMCTP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583095
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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