A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256167



Internal ID21400427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95794114..96032353hg38UCSC Ensembl
chr2:96459862..96698101hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38238240
hg19238240
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730084
Supporting Variants
SamplesNA19239
Known GenesFAHD2CP, GPAT2, LINC00342
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256167
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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