A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109894



Internal ID21494653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177297944..177297944hg38UCSC Ensembl
chr2:178162672..178162672hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623868
Supporting Variants
SamplesNA19238
Known GenesLOC100130691
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109894
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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