A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115519



Internal ID21422731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95801271..96023342hg38UCSC Ensembl
chr2:96467019..96689090hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38222072
hg19222072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665155
Supporting Variants
SamplesHG00731
Known GenesFAHD2CP, GPAT2, LINC00342
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115519
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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