A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115317



Internal ID21445789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:965203..965203hg38UCSC Ensembl
chr2:960889..960889hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613108
Supporting Variants
SamplesHG00732
Known GenesSNTG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115317
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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