A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631214



Internal ID21579519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75027968..75027968hg38UCSC Ensembl
chr5:74323793..74323793hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152176
SamplesNA19238
Known GenesGCNT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631214
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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