A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152176



Internal ID21494975
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 StatusS
Merged Variantsnsv5631214
Supporting Variants
SamplesNA19238
Known GenesGCNT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152176
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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