A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114051



Internal ID21423277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36505307..36505307hg38UCSC Ensembl
chr2:36732450..36732450hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609466
Supporting Variants
SamplesHG00731
Known GenesCRIM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114051
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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