A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132533



Internal ID21434275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76689356..76689356hg38UCSC Ensembl
chr4:77610509..77610509hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615733
Supporting Variants
SamplesHG00731
Known GenesSHROOM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132533
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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